Medline Industries, Inc. DYNDL1225Recalls & reported problems

Medline Industries, Inc. · LACERATION TRAY · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489365108), received between Jun 30, 2025 and Jun 30, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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 18, 2026.

Reports received per month

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

Most reported problems

Device problems

Component Missing1
Defective Component1
Device Damaged Prior to Use1

Patient problems

No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

MalfunctionJun 30, 2025Device Damaged Prior to Use; Defective Component; Component Missing
DEFECTIVE LACERATION TRAY- FORCEPS HAD PUNCTURED THROUGH PLASTIC PACKAGING; FORCEPS WERE MISSING RUBBER CLOSURE DEVICE. FORCEP TIP APPEARS DAMAGED. TWO SEPARATE TRAYS HAD FORCEPS WITH DAMAGED TIPS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22352623 ↗

Device details

UDI-DI	`10193489365108`
Brand	Medline Industries, Inc.
Model	DYNDL1225
Company	Medline Industries, Inc.
Product code	MCY · Wound dressing kit
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jul 26, 2023

Device type (GMDN): General surgical procedure kit, non-medicated, single-use

A typically non-dedicated collection of various surgical instruments, sometimes with dressings and/or other materials, but that does not contain pharmaceuticals, intended to be used during: 1) open abdominal surgery; 2) a range of open surgical procedures across multiple clinical specialties (non-dedicated); 3) non-orthopaedic trauma surgery; 4) minor dermatological surgery; or 5) cosmetic surgery below the head. As a kit that includes procedural devices, it is neither dedicated to surgical scrubbing, surgical patient preparation, nor anaesthesia, and is not a dedicated biopsy kit. This is a single-use device.

Other Wound dressing kit devices

Medline Industries, Inc. DYNDH1487A
Medline Industries, Inc. · Wound dressing kit
3 recalls0 reports
Medline Industries, Inc. DM1035
Medline Industries, Inc. · Wound dressing kit
2 recalls0 reports
Medline Industries, Inc. DYNDH1193
Medline Industries, Inc. · Wound dressing kit
2 recalls0 reports
Medline Industries, Inc. DYKMBNDL43
Medline Industries, Inc. · Wound dressing kit
2 recalls0 reports
Medline Industries, Inc. DYNDH1561
Medline Industries, Inc. · Wound dressing kit
2 recalls0 reports
Medline Industries, Inc. SUT13535
Medline Industries, Inc. · Wound dressing kit
2 recalls0 reports
Medline Industries, Inc. DYNJ47717A
Medline Industries, Inc. · Wound dressing kit
2 recalls0 reports
Medline Industries, Inc. DYNDC2733
Medline Industries, Inc. · Wound dressing kit
1 recall0 reports

All Wound dressing kit 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 18, 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