EASY CLIP EZB10-15-13Recalls & reported problems
Stryker GmbH · Osteosynthesis Compression Staple · Class 2 · Implant
All models of EASY CLIP (15)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613252259367), received between Jun 4, 2018 and Jun 4, 2018 — classified as 1 injury.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Nerve Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 4, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE SURGEON REPORTED : "LAST TUESDAY I OPERATED A PATIENT FOR A THP VIA DSA. THE PROCEDURE WENT SMOOTHLY, FOLLOWING THE TIPS FROM THE INSTRUCTIONAL GUIDE FROM STRYKER. POSTOPERATIVELY THE PATIENT DEVELOPED AN N FEMORALIS OUTAGE." THE CUSTOMER ASKS FOR ADVISE FROM AN EXPERT TO AVOID THIS IN THE FUTURE. UPDATE PER ADDITIONAL INFORMATION RECEIVED (B)(6) 2018 - DOCTOR DID A PRIMARY HIP WITH A TRITANIUM CUP AND A EXETER FEMORAL STEM . HE USED FOR THE APPROACH THE DSA TECHNIQUE , ( DIRECT SUPERIOR APPROACH ) WHICH IS PROMOTED BY US SINCE A COUPLE OF YEARS . AFTER THE OPERATION THE PATIENT HAD A FEMORALIS DROP , WHAT IS SOMETHING LIKE A PARALYSIS OF THE SCIATIC NERVE. THERE WAS NO REVISION.
Patient problems: Nerve Damage
MAUDE report 7567127 ↗
Other STAPLE, FIXATION, BONE devices
- N/A StandardSynthes GmbH · Staple, Fixation, Bone2 recalls16 reports
- GII QUICKANCHOR ETHIBOND 212034Medos International Sàrl · STAPLE, FIXATION, BONE98 reports
- GII QUICKANCHOR ORTHOCORD 222983Medos International Sàrl · STAPLE, FIXATION, BONE94 reports
- Speed SE-0910Synthes GmbH · Staple, Fixation, Bone1 recall24 reports
- Speed Shift SE-2020-10Synthes GmbH · Staple, Fixation, Bone1 recall10 reports
- Lapiplasty SpeedPlate SK50Treace Medical Concepts, Inc. · Staple, Fixation, Bone59 reports
- Speed SE-1512Synthes GmbH · Staple, Fixation, Bone1 recall6 reports
- LUPINE ORTHOCORD 210709Depuy Mitek, LLC · STAPLE, FIXATION, BONE56 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page