SPECIALIST 96-6515Recalls & reported problems
Depuy (Ireland) · SPECIALIST 2 PIN PULLER · Class 1
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 10603295248637), received between Feb 21, 2019 and Aug 6, 2026 — classified as 15 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (11 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.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility11
- Contamination /Decontamination Problem2
- Break1
- Corroded1
- Material Twisted/Bent1
- Mechanical Jam1
- Naturally Worn1
- Positioning Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
- No Consequences Or Impact To Patient5
- Insufficient Information2
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 6, 2026Corroded; Contamination /Decontamination Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50162881 ↗MalfunctionSep 27, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem
IT WAS REPORTED THAT DURING LOAN KIT INSPECTION, BY THE LOAN KIT TECHNICIAN IT WAS IDENTIFIED THAT THE DEVICE IS RUSTY. THERE IS NO SURGEON, PROCEDURE, OR PATIENT DETAILS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20323447 ↗MalfunctionSep 12, 2024Device-Device Incompatibility; Device-Device Incompatibility
THE PIN PULLER DOESN¿T GRIP ONTO THE PINS SO NEEDS TO BE REPLACED.
Patient problems: Insufficient Information
MAUDE report 20198920 ↗MalfunctionAug 5, 2024Device-Device Incompatibility; Device-Device Incompatibility
ADDITIONAL INFORMATION RECEIVED STATES THAT THE EVENT OCCURRED FOLLOWING INSTRUMENT STERILIZATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19906622 ↗MalfunctionMay 7, 2024Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
ADDITIONAL INFORMATION WAS RECEIVED: THE SPRING ON THE PIN PULLER HAD WORN OUT, SO IT WOULD NOT RELEASE THE PIN ONCE REMOVED FROM BONE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19264087 ↗MalfunctionApr 21, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE PIN PULLER WOULD NOT GRAB PINS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16788265 ↗MalfunctionMar 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE PIN PULLER WON¿T GRAB PIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16629275 ↗MalfunctionAug 22, 2022Device-Device Incompatibility; Device-Device Incompatibility
THE PIN PULLER WAS NO LONGER GRIPPING THE PINS. NO ADVERSE AFFECTS ON THE PATIENT. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15266540 ↗MalfunctionDec 10, 2021Break; Break
SPRING ON INSTRUMENT BROKEN DUE TO WEAR. NEW TRAY OPENED TO GET REPLACEMENT INSTRUMENT. 2 MINUTES DELAY TO SURGERY.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 12977697 ↗MalfunctionDec 2, 2020Device-Device Incompatibility; Material Twisted/Bent; Mechanical Jam; Device-Device Incompatibility; Material Twisted/Bent; Mechanical Jam
PIN PULLER HAS BECOME SPRUNG AND PINS ARE ABLE TO BE PULLED BUT THE PIN BECOMES STUCK IN THE INSTRUMENT. NOT DETRIMENTAL TO PATIENT JUST INCONVENIENCE TO CUSTOMERS UTILIZING INSTRUMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10936578 ↗MalfunctionOct 25, 2019Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE INSTRUMENT WON'T LOCK PINS IN.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9240808 ↗MalfunctionOct 25, 2019Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE INSTRUMENT WON'T LOCK PINS IN.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9240807 ↗MalfunctionSep 18, 2019Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SPRING WILL NOT RELEASED. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9081744 ↗MalfunctionAug 30, 2019Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SPECIALIST 2 PIN PULLER WILL NOT GRAB PINS. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8951804 ↗MalfunctionFeb 21, 2019Positioning Problem; Positioning Problem
IT WAS REPORTED THAT THE PIN PULLER WOULD NOT PULL THE PINS OUT. IT KEPT SLIPPING OFF. THERE WAS NO LOT NUMBER. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8359407 ↗
Other EXTRACTOR devices
- ATTUNE 2545-00-138Depuy (Ireland) · EXTRACTOR392 reports
- PINNACLE 2217-50-001Depuy (Ireland) · EXTRACTOR243 reports
- RECLAIM 2975-00-635Depuy (Ireland) · EXTRACTOR157 reports
- ATTUNE 2545-00-060Depuy (Ireland) · EXTRACTOR153 reports
- ESC PINNACLE 2218-00-010Depuy (Ireland) · EXTRACTOR151 reports
- NA 2125-00-600Depuy Orthopaedics, Inc. · EXTRACTOR130 reports
- P.F.C. 86-5226Depuy (Ireland) · EXTRACTOR80 reports
- NA 03.010.000Synthes GmbH · EXTRACTOR74 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.