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POSEY

POSEY PRODUCTS, LLC · Model A8070M · UDI-DI 10190676000989

OYS Prescription
3
510(k) clearances
474
Adverse events (8 deaths)
1
Recalls
10
Facilities

Description

8070 MATTRESS

Recalls

DateFirmReason
2022-03-14Sensory Medical IncDue potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.