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Howell

COOK INCORPORATED · Model G21791 · UDI-DI 00827002217911

FCK Prescription
10
510(k) clearances
17
Adverse events
1
Recalls
4
Facilities

Description

Howell Biliary Aspiration Needle

Recalls

DateFirmReason
2011-11-03Bard Peripheral Vascular IncThis recall was voluntarily initiated by the firm due to the product 's damaged packaging trays; cracked EnCor (Trademark) packaging trays, plastic PETG tray the probe is packaged

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Data 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.