NA 011022Recalls & reported problems
Smith & Nephew, Inc. · GRSPR FRCP LOOSEBODY PTBLL · Class 1
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 03596010023025), received between Jun 2, 2025 and Jun 2, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2025Break; Break
IT WAS REPORTED THAT DURING A KNEE ARTHROSCOPY, THE SURGEON WAS RETRIEVING A LOOSE BODY FROM PATIENT USING ONE (1) PITBULL GRASPER SIDELOCK HANDLE, AND THE INSTRUMENT BROKE AT THE TIP OF THE GRASPING SECTION. AN X-RAY WAS TAKEN AND THE BROKEN PART OF THE INSTRUMENT WAS AT THE POSTERIOR SIDE OF THE TIBIA, AND IT WAS UNABLE TO BE RETRIEVED. THERE WAS A SURGICAL DELAY GREATER THAN 30 MINUTES, AND THEN THE PROCEDURE WAS CANCELLED AND RESCHEDULED FOR ANOTHER SURGERY. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 22124971 ↗
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- NA 251723Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC145 reports
- COBRA 3910900093Stryker Corporation · Accessories, arthroscopic138 reports
- FirstPass 72290129Smith & Nephew, Inc. · Accessories, arthroscopic82 reports
- FirstPass 72290130Smith & Nephew, Inc. · Accessories, arthroscopic80 reports
- MITEK 242025Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC61 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.
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