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Curaplex MS-42210Recalls & reported problems

Bound Tree Medical, LLC · Curaplex XPS Fitted Sheet, 36 in x 90 in, Light Blue, 400lbs weight rating, 96gsm 30/CS · Class 1

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 00810071633331), received between Jul 20, 2023 and Jul 20, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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

  • Material Split, Cut or Torn1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionJul 20, 2023Material Split, Cut or Torn; Material Split, Cut or Torn

    DIRECTLY FROM THE CUSTOMER: "I LEARNED WE HAVE ONE GUY OFF ON INJURY FOR HAVING TO CATCH A PATIENT BECAUSE ONE OF THESE SHEETS TORE WHILE TRANSFERRING A PATIENT AT THE HOSPITAL."

    Patient problems: Insufficient Information

    MAUDE report 17367623 ↗

Other BEDDING, DISPOSABLE, MEDICAL devices

All BEDDING, DISPOSABLE, MEDICAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.