Medline Industries, Inc. MDS708555Recalls & reported problems
Medline Industries, Inc. · TRAY,SUTURE REMOVAL,MTL LITT · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10080196999040), received between Apr 22, 2026 and Sep 25, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Break” (3 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break3
- Dull, Blunt2
- Corroded1
- Material Discolored1
- Product Quality Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Dull, Blunt
It was reported that Scissors struggled to cut ostomy bag.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50897092 ↗MalfunctionSep 21, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50847051 ↗MalfunctionSep 18, 2026Product Quality Problem
It was reported that "inconsistent thickness and point on suture end of scissors, have to open multiple packs to find a pair of suture scissors small, thin and pointy enough to removed small sutures."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50817654 ↗MalfunctionSep 17, 2026Corroded; Material Discolored
It was reported that they have had about 20 now that have had an issue as far as them looking "rusty" in some areas or even having some kind of red fuzz on it.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50803218 ↗MalfunctionSep 15, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50779564 ↗MalfunctionSep 14, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50755449 ↗MalfunctionApr 22, 2026Break
IT WAS REPORTED ON 03/30 THAT THE SCISSORS INCLUDED IN A SUTURE REMOVAL TRAY BROKE DURING PATIENT USE. NO INJURY TO THE PATIENT WAS MENTIONED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24955693 ↗
Other TRAY, SURGICAL, INSTRUMENT devices
- PINNACLE 2220-00-100Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT74 reports
- ACTIS 2010-04-200Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT66 reports
- ATTUNE 2545-01-703Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT62 reports
- ATTUNE 2545-01-704Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT57 reports
- Calibrate CLCCXSIMPAAlphatec Spine, Inc. · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501BECKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501XKKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501A2Karl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
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.
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