Home › J & J INSTRUMENTS INC › J & J INSTRUMENTS INC
J & J INSTRUMENTS INC
J & J INSTRUMENTS INC · Model 02-360 · UDI-DI 00817524020540
3
510(k) clearances
73
Adverse events
1
Recalls
202
Facilities
Description
MEAD MALLET 7.5"" RUBBER-FACED
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.