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Posey
TIDI PRODUCTS, LLC · Model A8075B · UDI-DI 10618125191663
OYS
Prescription
3
510(k) clearances
462
Adverse events (8 deaths)
1
Recalls
10
Facilities
Description
8075 Bed
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-03-14 | Sensory Medical Inc | Due potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021. |
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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.