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Capette
WESTMED, INC. · Model CP-4202 · UDI-DI 00709078013003
JAY
Prescription
10
510(k) clearances
150
Adverse events
2
Recalls
72
Facilities
Description
Medium Capette™ with small tube tackles
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-10-20 | CooperSurgical, Inc. | Firm has received 11 complaints involving a loose or detached metal clips, including 3 cases where the metal clip was ingested by the patient, and 3 cases where the metal clip was |
| 2005-10-14 | Instrumentation Industries Inc | potential for the flexible tube portion of the assembly to become brittle and break |
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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.