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Hollister
HOLLISTER INCORPORATED · Model 9345 · UDI-DI 00610075093458
0
510(k) clearances
4
Adverse events
1
Recalls
34
Facilities
Description
Extension Tubing with connector
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-07-10 | Customed, Inc | Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile. |
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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.