Home › priMED Medical Products Inc › PRIMED
PRIMED
priMED Medical Products Inc · Model PM4-88335XL · UDI-DI 00842942015441
5
510(k) clearances
7
Adverse events (1 deaths)
1
Recalls
237
Facilities
Description
Overhead Film Gown / Thumbloop Cuff / Open Back / Universal / XL
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-12-23 | Encompass Group LLC | The products are not compatible for use in the Magnetic Resonance Imaging (MRI) environment. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.