QUICKSET 2274-64-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295109372), received between Jul 22, 2019 and Mar 4, 2026 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Peeled/Delaminated” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 4, 2026Peeled/Delaminated

  IT WAS REPORTED THAT THE TRAYS PEELING WOULD NOT STERILIZE. THE EVENT DID NOT HAPPEN IN SURGERY. (B)(4) IS RELATED TO (B)(4) IS CREATED TO CAPTURE ADDITIONAL IPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24510994 ↗
• MalfunctionMar 4, 2026Peeled/Delaminated

  IT WAS REPORTED THAT THE TRAYS PEELING WOULD NOT STERILIZE. THE EVENT DID NOT HAPPEN IN SURGERY. (B)(4) IS RELATED TO (B)(4). (B)(4) IS CREATED TO CAPTURE ADDITIONAL IPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24505205 ↗
• MalfunctionMar 4, 2026Peeled/Delaminated

  IT WAS REPORTED THAT THE TRAYS PEELING WOULD NOT STERILIZE. THE EVENT DID NOT HAPPEN IN SURGERY. (B)(4) IS RELATED TO (B)(4) IS CREATED TO CAPTURE ADDITIONAL IPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24505114 ↗
• MalfunctionJun 10, 2025Break; Contamination /Decontamination Problem; Break; Contamination /Decontamination Problem

  CONSIGNMENT REPLACEMENT TRAYS REQUIRED DUE TO STERILISATION CONCERNS FOR PINNACLE TRIAL SHELLS, SCREW TRAY, X BACK GRATERS QUICKSET GRATERS AND SHELL TRIALS. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22176458 ↗
• MalfunctionFeb 4, 2025Crack; Peeled/Delaminated; Crack; Peeled/Delaminated

  IT WAS REPORTED THAT THE HOSPITAL COMPLAINT ABOUT TRAYS CHIPPING, PEELING, CRACKING AND THE OUTER RUBBER PEELING OFF. IT WAS REPORTED THAT THE CHIPPING DID NOT HAPPEN IN SURGERY. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED FOR REPORTING. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21309088 ↗
• MalfunctionNov 13, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem

  IT WAS REPORTED THAT ALL THREE INNER TRAYS OF THE PINNACLE GREATER INSTRUMENT SET ARE STAINED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10839643 ↗
• MalfunctionJul 22, 2019Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  PINNAC ACETABULAR BOLT INSTRUMENTAL KIT 500008896, L001927, ACCUMULATED WATER INTERNALLY IN THE INSTRUMENT TRAYS. PINNACLE BOX OF BOLTS: CODE: 227464000, LOT: PV0173211.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8813607 ↗