Home › RZ-Medizintechnik GmbH › RZ Medizintechnik GmbH
RZ Medizintechnik GmbH
RZ-Medizintechnik GmbH · Model 430-130-070 · UDI-DI 04049197319362
GAC
Prescription
2
510(k) clearances
32
Adverse events
1
Recalls
180
Facilities
Description
Davis-Meyer tongue blades 29x70mm with tubing set for anaesthesia channel
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-12-29 | Stryker Howmedica Osteonics Corp. | Stryker Orthopaedics has become aware of the potential for the above noted Accolade Rasp Handle Assembly to fracture upon use. |
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.