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RZ Medizintechnik GmbH
RZ-Medizintechnik GmbH · Model 410-800-000 · UDI-DI 04049197310161
KYZ
Prescription
10
510(k) clearances
589
Adverse events (1 deaths)
20
Recalls
373
Facilities
Description
Ear syringe, 10 ml, all metal chromium plated, for easy continous one hand filling and emptying, Luer-Lock attachme
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.