WECK IPN028496Recalls & reported problems
Teleflex Incorporated · DURAHOOK 1/4 HOOK 10 PACKAGES PER BOX /6 HOOKS PER PACKAGE · Class 1
All models of WECK (97)
Data updated Oct 16, 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 14026704631749), received between Jan 8, 2024 and Jan 8, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 8, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT "METAL HOOK PART DETACHES FROM ELASTIC AND BREAKS OFF WHILE SURGEON IS USING IT". AT THE TIME OF THIS REPORT, THE CUSTOMER HAS NOT RETURNED OUR REQUESTS FOR ADDITIONAL INFORMATION. IF FURTHER INFORMATION IS RECEIVED, THE COMPLAINT FILE WILL BE UPDATED.
Patient problems: Insufficient Information
MAUDE report 18467198 ↗
Other INSTRUMENT, SURGICAL, NON-POWERED devices
- SenSight™ B31030Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED1 recall7 reports
- WECK IPN006432Teleflex Incorporated · INSTRUMENT, SURGICAL, NON-POWERED3 reports
- NA 1120Advanced Neuromodulation Systems, Inc. · INSTRUMENT, SURGICAL, NON-POWERED2 reports
- 3.3mm Mini-Bolt VUE 21133Monteris Medical Inc · INSTRUMENT, SURGICAL, NON-POWERED2 reports
- NA 365538Medtronic, Inc. · INSTRUMENT, SURGICAL, NON-POWERED2 reports
- Integra® Jarit® 285120Integra Lifesciences Production Corporation · INSTRUMENT, SURGICAL, NON-POWERED1 report
- OASYS 48561039Stryker Corporation · INSTRUMENT, SURGICAL, NON-POWERED1 report
- AESCULAP FV002RAesculap AG · INSTRUMENT, SURGICAL, NON-POWERED1 report
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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