Halyard 44915Recalls & reported problems
Avanos Medical, Inc. · Acute Pain, ON-Q-TBLOC, PRPTRY, 5 · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10680651449150), received between Dec 7, 2017 and Dec 7, 2017 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 7, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION RECEIVED 04-DEC-2017 STATED THE ANESTHESIOLOGIST CONFIRMED THAT THE PATIENT'S CONDITION WAS RESOLVING AS SHE WAS DISCHARGED ON (B)(6) 2017.THE ANESTHESIOLOGIST ALSO THINKS THAT THE CONDITION WAS NOT A TRUE INFECTION BUT A REACTION. NO MEDICAL DIAGNOSIS WAS OBTAINED.
Patient problems: Unspecified Infection
MAUDE report 7098604 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.