Home › E.M. ADAMS, INC. › E.M Adams co, inc.
E.M Adams co, inc.
E.M. ADAMS, INC. · Model 3030 · UDI-DI 50840200304783
1
510(k) clearances
6
Adverse events
1
Recalls
64
Facilities
Description
UNIVERSAL KNEE SPLINT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-02-27 | Emergency Products & Research | Failure of adhesive to secure the pole insert. |
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.