ATRAUMATA FB568RRecalls & reported problems
Aesculap AG · COOLEY ATRAUMATA Vascular Clamp, angled, 60 °, 6 1/4", (160 mm), pediatric pattern, toothing DE BAKEY, (30 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-1311-2025 · Root cause: Use error · FDA record ↗
Other CLAMP devices
- ATTUNE 2544-00-001Depuy (Ireland) · CLAMP144 reports
- NA 2178-63-134Depuy (Ireland) · CLAMP137 reports
- ATTUNE 2545-01-055Depuy (Ireland) · CLAMP128 reports
- SPECIALIST 86-5035Depuy (Ireland) · CLAMP101 reports
- SPECIALIST 96-6670Depuy Orthopaedics, Inc. · CLAMP92 reports
- Centurion I68080Centurion Medical Products Corporation · CLAMP1 recall0 reports
- Centurion I68095Centurion Medical Products Corporation · CLAMP1 recall0 reports
- Centurion ZC110STCenturion Medical Products Corporation · CLAMP1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.