Home › RZ-Medizintechnik GmbH › RZ Medizintechnik GmbH
RZ Medizintechnik GmbH
RZ-Medizintechnik GmbH · Model 210-681-001 · UDI-DI 04049197508490
HTS
Prescription
9
510(k) clearances
12
Adverse events
3
Recalls
117
Facilities
Description
Tenolysis Knife Style A for tenolysis superficial & deep to the tendon
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-09-30 | Beaver Visitec International, Inc. | Incorrect configuration of the blades in the package. The blades curve to the right instead of curving to the left. If used may cause cause unintended tissue damage during the proc |
| 2009-11-11 | Stryker Howmedica Osteonics Corp. | Disposable Patella Cutters - 30 mm (catalog number 8000-0030, lot V31257001) were packaged and labeled as 33 mm Disposable Patella Cutters (catalog number 8000-0033, lot V31257001 |
| 2009-06-12 | Becton Dickinson and Company | Mislabeled: Arthro-Lok Pointed Tip 4mm Blade curving right instead of left. |
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.