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Amimon
Rocoto Inc. · Model HM11 Device - MDWL1_HM11 · UDI-DI 00860014100680
0
510(k) clearances
12
Adverse events
1
Recalls
71
Facilities
Description
HM11 Device
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-06-11 | Integra LifeSciences Corp. | LED battery chargers may prematurely fail and will not charge the LED battery as intended |
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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.