NA 0250080767Recalls & reported problems
Stryker Corporation · Sliding-Lock Atraumatic Grasper, Double Action. · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 07613327056648), received between Aug 9, 2018 and Apr 4, 2025 — classified as 5 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Break” (7 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break7
- Material Fragmentation2
- Mechanical Problem1
Patient problems
- No Known Impact Or Consequence To Patient4
- Device Embedded In Tissue or Plaque3
- No Clinical Signs, Symptoms or Conditions2
- Foreign Body In Patient1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjuryApr 4, 2025Break; Material Fragmentation; Break; Material Fragmentation
IT WAS REPORTED THAT THE DEVICE BROKE AND CANNOT CONFIRM IF ALL THE BROKEN PIECES WERE SUCCESSFULLY REMOVED FROM THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21774653 ↗InjuryMar 8, 2022Break
IT WAS REPORTED THAT A PIECE OF THE PRODUCT BROKE AND REMAINED IN THE PATIENT.
Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions
MAUDE report 13691182 ↗MalfunctionOct 29, 2019Break
IT WAS REPORTED THAT THE PLASTIC SHEATH ON WAVE GRASPER BROKE INTRAOPERATIVELY, ALL PIECES WERE RETRIEVED AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9251636 ↗MalfunctionJul 29, 2019Mechanical Problem; Break; Mechanical Problem
IT WAS REPORTED THAT THE DEVICE BROKE DURING THE PROCEDURE. PER ADDITIONAL INFORMATION RECEIVED, AN X-RAY WAS PERFORMED AND CAME BACK NEGATIVE THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8837171 ↗InjuryJan 7, 2019Material Fragmentation
IT WAS REPORTED THAT A PIECE OF THE GRASPER REMAINED INSIDE OF THE PATIENT. PLEASE NOTE THAT THE SURGEON ELECTED NOT TO PERFORM THE XRAY.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 8224237 ↗InjuryJan 3, 2019Break
IT WAS REPORTED THAT A PIECE OF GRASPER REMAINED INSIDE THE PATIENT.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 8214937 ↗InjuryAug 17, 2018Break
IT WAS REPORTED THAT THE SCREW BROKE AND WAS POTENTIALLY LEFT INSIDE OF THE PATIENT.
Patient problems: Device Embedded In Tissue or Plaque; No Known Impact Or Consequence To Patient
MAUDE report 7795336 ↗MalfunctionAug 9, 2018Break
IT WAS REPORTED THAT THE GRASPER BROKE DURING A CASE. PER ADDITIONAL INFORMATION RECEIVED, ALL PIECES WERE RETRIEVED AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7770496 ↗
Other FORCEPS, GENERAL & PLASTIC SURGERY devices
- Centurion 67870Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY2 recalls2 reports
- MEDLINE DYNJ04048Medline Industries, Inc. · FORCEPS, GENERAL & PLASTIC SURGERY2 recalls0 reports
- Centurion 66790Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY2 recalls0 reports
- Centurion I68420Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Sklar Instruments 96-2549Sklar Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall2 reports
- Centurion 66195Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion 67310Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 report
- Centurion 66440Centurion Medical Products Corporation · FORCEPS, GENERAL & PLASTIC SURGERY1 recall1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page