POSEY 2790QRecalls & reported problems
Posey Products, LLC · POSEY TAT, WRIST · Class 1
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 10190676003379), received between Nov 26, 2024 and Nov 26, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionNov 26, 2024Break; Break
REPORTED VIA FDA (B)(4). COMPLAINT DESCRIPTION: WRIST RESTRAINT WAS BORROWED FROM ONE OF OUR OTHER INPATIENT USER FACILITIES. DURING ATTEMPT TO APPLY RESTRAINTS TO A COMBATIVE PATIENT, STAFF WERE TRYING TO SECURE THE RESTRAINT TO THE BED WHEN THE PLASTIC SNAP ON THE WRIST RESTRAINT BROKE AND MADE THE RESTRAINT UNUSABLE. A NEW RESTRAINT WAS APPLIED TO THE PATIENT'S WRIST. PER NURSING LEADERSHIP REVIEW, THE RESTRAINTS WERE APPLIED CORRECTLY AND ADDITIONAL RESTRAIN EDUCATION IS BEING PROVIDED. THE TRIANGLES ON THE NORIX PLATFORM BED WERE NOT BEING UTILIZED DURING THE ABOVE EVENT. PRODUCT IS NOT AVAILABLE FOR RETURN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20785533 ↗
Other Restraint, Protective devices
- DeRoyal M8138Deroyal Industries, Inc. · Restraint, protective1 recall1 report
- DeRoyal M8137Deroyal Industries, Inc. · Restraint, protective1 recall0 reports
- DeRoyal M8136Deroyal Industries, Inc. · Restraint, protective1 recall0 reports
- DeRoyal M8125Deroyal Industries, Inc. · Restraint, protective1 recall0 reports
- DeRoyal M8124Deroyal Industries, Inc. · Restraint, protective1 recall0 reports
- POSEY 2532Posey Products, LLC · Restraint, Protective36 reports
- POSEY 2551Posey Products, LLC · Restraint, Protective14 reports
- POSEY 2799Posey Products, LLC · Restraint, Protective9 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.
How reports and recalls are matched · Editorial policy · Report an error on this page