Home › RZ-Medizintechnik GmbH › RZ Medizintechnik GmbH
RZ Medizintechnik GmbH
RZ-Medizintechnik GmbH · Model 130-012-200 · UDI-DI 04049197043243
GEN
Prescription
10
510(k) clearances
673
Adverse events (3 deaths)
10
Recalls
452
Facilities
Description
Standard Dressing Forceps slender, straight, 200mm, 8"
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2024-11-12 | MEDLINE INDUSTRIES, LP - Northfield | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. |
| 2024-11-12 | MEDLINE INDUSTRIES, LP - Northfield | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
| 2018-09-20 | Micro-Tech (Nanjing) Co., Ltd. | Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units |
| 2016-10-28 | Integra York PA, Inc | The Chevron seals of 6x10 Tyvek peel pouch used to package the sterile instruments may separate causing the packages to open and compromise sterility of the instrument. |
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
| 2010-06-25 | Biomet Microfixation, Inc. | The forceps insulation may have cracks or breaks in the insulation that may cause burns to patients when used. |
| 2003-08-29 | Cordis Corporation | Some devices may have an incorrect inner label which shows Product # 504302L with a length of 50cm, while the outer label is correctly labeled as Product # 504300L with the length |
| 2003-08-29 | Cordis Corporation | Some devices may have an incorrect inner label which shows Product # 504302L with a length of 50cm, while the outer label is correctly labeled as Product # 504300L with the length |
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.