AESCULAP BJ534RRecalls & reported problems
Aesculap AG · GWILLIAM Hysterectomy Forceps, straight, 8", (200 mm), toothed (1x2), non-sterile, reusable · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Jan 31, 2025Open, Classified
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Z-1308-2025 · Root cause: Use error · FDA record ↗
Other CLAMP, UTERINE devices
- AESCULAP MD591Aesculap AG · CLAMP, UTERINE1 recall0 reports
- AESCULAP BJ530RAesculap AG · CLAMP, UTERINE1 recall0 reports
- ATRAUMATA BJ553RAesculap AG · CLAMP, UTERINE1 recall0 reports
- AESCULAP BJ532RAesculap AG · CLAMP, UTERINE1 recall0 reports
- AESCULAP MD592Aesculap AG · CLAMP, UTERINE1 recall0 reports
- AESCULAP BJ520RAesculap AG · CLAMP, UTERINE1 recall0 reports
- AESCULAP BJ531RAesculap AG · CLAMP, UTERINE1 recall0 reports
- AESCULAP BJ524RAesculap AG · CLAMP, UTERINE1 recall0 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 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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