AnchorFastRecalls & reported problems across all models

We found 2 models of AnchorFast by Hollister Incorporated in the FDA's device registry (GUDID). Together they are named in 70 adverse event reports in the FDA's MAUDE database, received between Aug 10, 2021 and Jun 23, 2026 — classified as 1 death, 54 injuries, 15 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (8 reports).

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

AnchorFast recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Dec 23, 2024Open, Classified

   Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

   Z-1180-2025 · Root cause: Process change control · Recall details · FDA record ↗

Most reported AnchorFast problems

AnchorFast models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• AnchorFast 9799

  DEVICE, FIXATION, TRACHEAL TUBE
  1 recall1 death49 reports
• AnchorFast 9799

  DEVICE, FIXATION, TRACHEAL TUBE
  21 reports

Recent AnchorFast adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjuryJun 23, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE FAMILY REMOVED WRIST RESTRAINTS AND PATIENT PULLED TUBE OUT.

  Patient problems: Unintended Extubation

  MAUDE report 25599735 ↗
• InjuryJun 23, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT'S ENDOTRACHEAL TUBE (ETT) BECAME DISLODGED DURING A COUGHING EPISODE. THE REGISTERED NURSE RESPONDED AND OBSERVED THAT THE ETT AND HOLLISTER'S ANCHORFAST ORAL ENDOTRACHEAL TUBE FASTENER HAD DETACHED FROM THE PATIENT. THE PATIENT REQUIRED REINTUBATION, NO OTHER DETAILS ARE AVAILABLE AT THIS TIME REGARDING THIS REPORTED EVENT.

  Patient problems: Unintended Extubation

  MAUDE report 25599461 ↗
• InjuryMay 13, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED IN THE MEDWATCH THAT THE PATIENT SUSTAINED A PRESSURE INJURY TO THE UPPER LIP, LIKELY FROM MECHANICAL VENTILATION/ETT HOLDER (ANCHOR FAST). IN ADDITION, IT WAS REPORTED IN THE MEDWATCH THAT NECROTIC TISSUE EXTENDED FROM THE LIP INTO THE MUCOSAL SURFACE OF THE INNER LIP. FURTHER, IT WAS REPORTED IN THE MEDWATCH THAT NECROSIS ON THE UPPER LIP WOUND WAS HEALING BUT FULL THICKNESS DEFECT REMAINED. IT WAS REPORTED IN THE MEDWATCH THAT DEBRIDEMENT WAS COMPLETED ON THE UPPER LIP OPEN WOUND AND RECONSTRUCTION WITH COMPLEX LAYERED CLOSURE WAS COMPLETED.

  Patient problems: Pressure Sore/Ulcer

  MAUDE report 25161847 ↗
• InjuryApr 3, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 11 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN JUNE 2025 AND JANUARY 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24777368 ↗
• InjuryApr 3, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 5 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24777367 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 13 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN JUNE 2025 AND JANUARY 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766053 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 14 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766052 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 17 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766051 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 16 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN JUNE 2025 AND JANUARY 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766050 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 15 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766049 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 10 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766046 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 9 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766045 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 12 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766043 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 4 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766042 ↗
• InjuryApr 2, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS 8 OUT OF 17 REPORTS. IT WAS REPORTED THAT THIS FACILITY OBSERVED AN INCREASE IN UNPLANNED ENDOTRACHEAL TUBE EXTUBATIONS WHILE THE ANCHORFAST ENDOTRACHEAL TUBE FASTENER WAS IN USE. IT WAS REPORTED THAT THE FACILITY DID NOT OBSERVE ANY DEVICE MALFUNCTION AND THEY ARE NOT SURE WHY THE UNPLANNED EXTUBATIONS HAPPENED. IT WAS FURTHER REPORTED THAT THERE WERE 17 UNPLANNED EXTUBATIONS THAT OCCURRED BETWEEN (B)(6) 2025 AND (B)(6) 2026. IT WAS REPORTED THROUGH CHART REVIEWS THAT THE PATIENT'S LEVEL OF SEDATION RANGED FROM MILD TO SEDATED, THE ANCHORFAST NECK STRAPS WERE IN USE, UNABLE TO DETERMINE HOW THE VENTILATOR CIRCUITS WERE SUPPORTED, ONLY ONE INCIDENT REPORTED FREQUENT DEVICE CHANGES DUE TO CLAMMY SKIN, BUT OTHERWISE, THEIR PRACTICE IS TO CHANGE THE ANCHORFAST DEVICE EVERY 48 HOURS AND AS NEEDED, AND THAT 2 OF THE 17 PATIENTS WERE BEING TURNED AT THE TIME OF THE UNPLANNED EXTUBATION. HOLLISTER IS WORKING WITH THE ACCOUNT TO PROVIDE TRAINING AND INSERVICING AS NEEDED.

  Patient problems: Insufficient Information

  MAUDE report 24766041 ↗

Other Hollister Incorporated products

• Onli16 models · 8 reports · 1 recall
• AnchorFast Guard2 models · 6 reports · 1 recall
• New Image19 models · 28 reports