POSEY 2792Recalls & reported problems
Posey Products, LLC · POSEY TWICE AS TOUGH · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190676002716), received between Apr 19, 2023 and Feb 25, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (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
- Mechanical Problem1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 25, 2026Use of Device Problem
CUSTOMER REPORTED MULTIPLE OFFICERS ENDING UP WITH THUMB INJURIES FROM TRYING TO GET THE RESTRAINTS CLOSED. RECOMMENDATIONS ON THE IFU WERE FOLLOWED. WHAT WE HAVE FOUND IS THAT THE BUCKLE WORKS FINE ON ITS OWN, BUT ONCE THE STRAP IS FED THROUGH THE BUCKLE, WHEN OUR OFFICERS ARE ATTEMPTING TO PUSH THE BUCKLE CLOSED TO LOCK IT, IT HAS BECOME EXTREMELY DIFFICULT OR IMPOSSIBLE TO GET THEM TO ACTUALLY CLOSE AND LOCK INTO PLACE. WHAT WE HAVE SEEN IS DUE TO THE PRESSURE REQUIRED TO PUSH THE BUCKLES CLOSED, IT IS CAUSING STRAIN ON THE THUMBS WHICH HAS CREATED SORENESS AND STIFF- NESS. NO PRODUCT WILL BE RETURNED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24447291 ↗MalfunctionApr 19, 2023Mechanical Problem; Mechanical Problem
CUSTOMER REPORTS A COMPLAINT ON PRODUCT # 2792, 2793, 2794, & 2795. CUSTOMER STATES THAT PATIENTS ARE ABLE TO GET OUT OF THE RESTRAINT CUFFS. STAFF WAS ABLE TO DEMOSTRATE THAT THE D-RING WAS ABLE TO FIT INSIDE ITSELF AND RELEASE. STAFF REPORTED THAT THIS CAN HAPPEN WHEN THEY TIGHTEN THE RESTRAINT AND THE PATIENT CAN ALSO RELEASE THE RESTRAINT WITH THEIR TEETH. LOT# 2792 - 1251T055, 2794 - 2228T047, & 2793 - 2083T023 & 2220T109.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16773615 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.