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Penile Clamp
C. R. Bard, Inc. · Model 000433 · UDI-DI 00801741049002
FHA
Prescription
10
510(k) clearances
26
Adverse events
1
Recalls
70
Facilities
Description
Penile Clamp
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-02-16 | Aesculap Implant Systems LLC | The plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.