POSEY 2700QRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10190676002792), received between Aug 29, 2023 and Jun 24, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (4 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 24, 2026Break

  CUSTOMER IS REPORTING A COMPLAINT ON PRODUCT 2700Q RESTRAINT. CUSTOMER STATES DURING EDUCATION/TRAINING THAT THE PUSH DOWN PART THAT RELEASES THE BUCKLE BROKE OFF DURING NORMAL USAGE. TM STATES THAT THE DEVICE HAS BEEN USED NUMEROUS TIMES FOR TRAININGS. SOME CONCERN WAS RAISED OVER REPETITIVE/LONG TERM USE AND ANY RECOMMENDED USEFUL LIFE INFORMATION. NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25610392 ↗
• MalfunctionAug 23, 2024Break; Break

  CUSTOMER REPORTED ISSUE WITH PART 2700Q, ON (B)(6) 2024 AT 10:38PM A PATIENT WAS SLAMMING AND PRESSING THE GRAY PORTION OF THE BUCKLE AGAINST THE BED AND IT CRACKED THE BUCKLE. NO INJURY OR INCIDENT. ITEM IS NOT AVAILABLE FOR INSPECTION AS ITEM WAS DISCARDED, LOT NUMBER REPORTED WAS NEXT ON CUSTOMERS SHELF LOT NUMBER 4022T003.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20054012 ↗
• MalfunctionNov 22, 2023Break; Break

  CUSTOMER IS REPORTING COMPLAINT ON PRODUCT # 2700Q 2700QL. THE CUSTOMER IS STATING THAT PATIENTS ARE RIPPING THROUGH THE THIN PART OF THE MATERIAL. THE STAFF DID NOT WITNESS HOW IT HAPPENED AND IT WAS DISCOVERED DURING 15 MIN SAFETY CHECK.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18193362 ↗
• MalfunctionAug 29, 2023Break; Break

  (B)(6) REPORTED THEY HAVE 3 RESTRAINTS FROM THE SAME LOT NUMBER THAT HAVE BROKEN WHILE BEING USED ON COMBATIVE PATIENTS. ITEM # 2700Q LOT # 3135T004 LIMITED INFORMATION PROVIDED. REQUESTING PRODUCTS BE SENT IN FOR QA EVALUATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17644431 ↗