AESCULAP BH959RRecalls & reported problems
Aesculap AG · SCHNIDT Tonsil Forceps, curved, 7 1/4", (185 mm), non-sterile, reusable · Class 1
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-1312-2025 · Root cause: Use error · FDA record ↗
Other FORCEPS, ENT devices
- AESCULAP BH952RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH965RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH957RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH961RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH951RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH963RAesculap AG · FORCEPS, ENT1 recall0 reports
- Integra® 3711063Integra Lifesciences Production Corporation · FORCEPS, ENT2 reports
- V. Mueller RH551-111Steris Corporation · FORCEPS, ENT2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.