MEDLINE MSC3322Recalls & reported problems

Medline Industries, Inc. · GENTAC BRD GZE,2" X 2",1"X1"PAD, STERILE · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports: 2
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277720763), received between Sep 9, 2026 and Sep 21, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Delivered as Unsterile Product” (1 report).

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.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Delivered as Unsterile Product1
Packaging Problem1

Patient problems

No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

MalfunctionSep 21, 2026Packaging Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50842341 ↗
MalfunctionSep 9, 2026Delivered as Unsterile Product
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50697329 ↗

Device details

UDI-DI	`10888277720763`
Brand	MEDLINE
Model	MSC3322
Company	Medline Industries, Inc.
Product code	NAC · Dressing, wound, hydrophilic
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Apr 10, 2026

Device type (GMDN): Exudate-absorbent dressing, non-gel, non-antimicrobial

A wound covering intended to assist in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) and often by creating a moist wound-healing environment. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudates, but may be designed to absorb and remove exudates (e.g., by capillary action); it does not contain an antimicrobial agent, but may include antioxidant properties. The device is available in a variety of forms (e.g., flat sheet/film-like, impregnated pouches, filled sachets, lyophilized matrix, ribbon, rope, foam, liquid, or powder). After application, this device cannot be reused.

Other Dressing, wound, hydrophilic devices

MEDLINE INDUSTRIES, INC. MSC7044EP
Medline Industries, Inc. · Dressing, wound, hydrophilic
1 recall1 report
McKesson Reinforced Alginate
Advanced Medical Solutions Limited · Dressing, Wound, Hydrophilic
1 recall0 reports
McKesson 3563
Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic
1 recall0 reports
MAXORB EXTRA Alginate
Medline Industries, Inc. · Dressing, Wound, Hydrophilic
1 recall0 reports
DuPad® 87810
Derma Sciences Canada Inc · Dressing, wound, hydrophilic
1 recall0 reports
McKesson 87400
Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic
1 recall0 reports
McKesson 3562
Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic
1 recall0 reports
McKesson 3564
Mckesson Medical-Surgical Inc. · Dressing, Wound, Hydrophilic
1 recall0 reports

All Dressing, wound, hydrophilic devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

How reports and recalls are matched · Editorial policy · Report an error on this page