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RITEAID
RITE AID CORPORATION · Model 079573101988 · UDI-DI 00011822820134
10
510(k) clearances
5
Adverse events
1
Recalls
9
Facilities
Description
RITEAID MOTION BAND
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-04-26 | Psi Health Solutions | Product was marketed before its 510(k) application cleared. |
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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.