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CAREX HEALTH BRANDS
COMPASS HEALTH BRANDS CORP. · Model FGE80000 0000 · UDI-DI 00023601088000
10
510(k) clearances
15
Adverse events (2 deaths)
1
Recalls
103
Facilities
Description
CAREX NON-TILT OVERBED TABLE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-05-30 | Chattanooga Corp. | Product contains an improper bracket for the transducer. |
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.
