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BIOS Living
Thermor Ltd · Model LK022 · UDI-DI 00057475210229
5
510(k) clearances
1
Adverse events
1
Recalls
71
Facilities
Description
Latex Finger Cots, Box of 144 medium sized
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-03-31 | American Surgical Company | Product packaging defective compromising sterility |
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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.