Home › Princeton Medical Group, Inc. › PRINCETON
PRINCETON
Princeton Medical Group, Inc. · Model 33700-06 · UDI-DI 00810158218482
3
510(k) clearances
74
Adverse events
1
Recalls
202
Facilities
Description
MALLET HEATH 40MMØ 700G (1.54LBS) 7"
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-07-21 | Implant Resource Inc | Potential for mallet head to become separated from mallet handle. There is also significant deformations on striking surface that were not expected |
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.