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AKRUS
AKRUS GmbH & Co. KG · Model AK 5010MBS · UDI-DI 04260647941517
8
510(k) clearances
90
Adverse events (1 deaths)
1
Recalls
45
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-11-14 | TransMotion Medical Inc | The firm is finding that the stretcher chair controllers are moving the chairs involuntarily. |
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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.