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RZ Medizintechnik GmbH
RZ-Medizintechnik GmbH · Model 410-810-000 · UDI-DI 04049197310239
KYZ
Prescription
10
510(k) clearances
586
Adverse events (1 deaths)
20
Recalls
373
Facilities
Description
Aural cleaning tube, Cerumex
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-30 | Boston Scientific Corporation | Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loo |
| 2024-01-04 | MEDLINE INDUSTRIES, LP - Northfield | Packaging material was updated for the Bulb Irrigation Syringe (DYND20125), and additional testing done at Medline Corporate indicated the potential for the sterile barrier to be b |
| 2023-12-04 | Cardinal Health 200, LLC | Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist. |
| 2022-12-07 | MEDLINE INDUSTRIES, LP - Northfield | The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile. |
| 2018-02-06 | Baxter Healthcare Corporation | Affected lot of 5 mL oral dispensers was packaged in individual pouches that are mislabeled with the incorrect product code (H93876101) and volume (1mL). |
| 2017-12-19 | Cook Inc. | Certain lots of in vitro fertilization (IVF) products were distributed without completed finished device quality testing with potential adverse events that may include nonviable ga |
| 2017-06-01 | Shippert Medical Technologies | Seal integrity of the Tissu-Trans product sterile packages cannot be assured. |
| 2017-06-01 | Shippert Medical Technologies | Seal integrity of the Tissu-Trans product sterile packages cannot be assured. |
| 2016-08-03 | C.R. Bard, Inc. | Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility. |
| 2016-08-03 | C.R. Bard, Inc. | Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility. |
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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.