Medichoice ORT04BRecalls & reported problems
Owens & Minor Distribution, Inc. · Towel Operating Room Pre-Washed De-Linted Cotton Blue 16 X 24 Inch Disposable 4 Pack Sterile Not Made With Natural Rubber Latex MediChoice · Class 2
Data updated Oct 13, 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 10885632101724), received between Dec 1, 2017 and Dec 1, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Device Contamination with Chemical or Other Material1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 1, 2017Device Contamination with Chemical or Other Material
A HAIR WAS FOUND INSIDE THE STERILE PACKAGE OF A DISPOSABLE OR TOWEL. THIS WAS DISCOVERED PRIOR TO THE TOWELS BEING INTRODUCED TO THE STERILE FIELD. THE CONTAMINATED PACKAGE WAS REMOVED AND REPLACED. THE PROCEDURE WAS COMPLETED AS PLANNED WITH NO PATIENT CONTAMINATION. PER SITE REPORTER: RESPONSE FROM THE MANUFACTURER IS STILL PENDING. WE WILL RETURN PACK FOR INVESTIGATION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7074294 ↗
Other Drape, surgical devices
- Medline DYNJP8002Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2414RMedline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2411Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2410Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2416Medline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP3008UGMedline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP8201UGMedline Industries, Inc. · Drape, surgical2 recalls0 reports
- Medline DYNJP2412TMedline Industries, Inc. · Drape, surgical2 recalls0 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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