Halyard 45799Recalls & reported problems

Summary

The FDA's MAUDE database contains 20 adverse event reports that list this exact device (DI 10680651457995), received between Nov 17, 2019 and Nov 19, 2019 — classified as 5 deaths, 15 injuries.

The most frequently reported specific device problem is “Malposition of Device” (20 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 20 most recent of 20 reports, in the reporter's own words as published by the FDA.

• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE FIFTEENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9344750 ↗
• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE NINETEENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9344748 ↗
• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE SIXTEENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9344747 ↗
• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE EIGHTEENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9344746 ↗
• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE TWENTIETH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. AN FDA MEDWATCH

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9344726 ↗
• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE SEVENTEENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9344721 ↗
• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE FOURTEENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9340772 ↗
• InjuryNov 19, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE THIRTEENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9340767 ↗
• InjuryNov 18, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE SIXTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9339381 ↗
• InjuryNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE EIGHTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333477 ↗
• DeathNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE ELEVENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333476 ↗
• InjuryNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE SEVENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333475 ↗
• DeathNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE NINTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333474 ↗
• DeathNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE TENTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333473 ↗
• InjuryNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE TWELFTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333472 ↗
• DeathNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE SECOND OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Death; Pneumothorax

  MAUDE report 9333471 ↗
• DeathNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE FOURTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Death; Pneumothorax

  MAUDE report 9333470 ↗
• InjuryNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE FIRST OF TWENTY REPORTS. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333468 ↗
• InjuryNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE THIRD OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00220 FOR THE FIFTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333467 ↗
• InjuryNov 17, 2019Malposition of Device; Malposition of Device

  AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWENTY DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWENTY DIFFERENT EVENTS. THIS IS THE FIFTH OF TWENTY REPORTS. REFER TO 9611594-2019-00216 FOR THE FIRST EVENT. REFER TO 9611594-2019-00217 FOR THE SECOND EVENT. REFER TO 9611594-2019-00218 FOR THE THIRD EVENT. REFER TO 9611594-2019-00219 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00221 FOR THE SIXTH EVENT. REFER TO 9611594-2019-00222 FOR THE SEVENTH EVENT. REFER TO 9611594-2019-00223 FOR THE EIGHTH EVENT. REFER TO 9611594-2019-00224 FOR THE NINTH EVENT. REFER TO 9611594-2019-00225 FOR THE TENTH EVENT. REFER TO 9611594-2019-00226 FOR THE ELEVENTH EVENT. REFER TO 9611594-2019-00227 FOR THE TWELFTH EVENT. REFER TO 9611594-2019-00228 FOR THE THIRTEENTH EVENT. REFER TO 9611594-2019-00229 FOR THE FOURTEENTH EVENT. REFER TO 9611594-2019-00230 FOR THE FIFTEENTH EVENT. REFER TO 9611594-2019-00231 FOR THE SIXTEENTH EVENT. REFER TO 9611594-2019-00232 FOR THE SEVENTEENTH EVENT. REFER TO 9611594-2019-00233 FOR THE EIGHTEENTH EVENT. REFER TO 9611594-2019-00234 FOR THE NINETEENTH EVENT. REFER TO 9611594-2019-00235 FOR THE TWENTIETH EVENT. AN FDA MEDWATCH

  Patient problems: Pneumothorax

  MAUDE report 9333466 ↗