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Gimmi
Gimmi GmbH · Model AC.1532.23 · UDI-DI 04049047012702
GDJ
Prescription
10
510(k) clearances
300
Adverse events (3 deaths)
9
Recalls
270
Facilities
Description
MAYO-GUYON KIDNEY PEDICLE CLAMP LENGTH 230 MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2024-05-16 | Medtronic Perfusion Systems | Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set. |
| 2024-03-19 | Medtronic Perfusion Systems | Potential for unsealed sterile packing. |
| 2018-06-29 | Integra LifeSciences Corp. | There is a potential for the knob assembly in the swivel adapter to fracture/break during use. |
| 2018-06-29 | Integra LifeSciences Corp. | There is a potential for the knob assembly in the swivel adapter to fracture/break during use. |
| 2018-06-29 | Integra LifeSciences Corp. | There is a potential for the knob assembly in the swivel adapter to fracture/break during use. |
| 2018-06-29 | Integra LifeSciences Corp. | There is a potential for the knob assembly in the swivel adapter to fracture/break during use. |
| 2013-07-02 | Stryker Howmedica Osteonics Corp. | Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument. |
| 2005-04-06 | Smith & Nephew, Inc., Endoscopy Div. | Cupped Grasper Handle marked incorrectly as Duckbill Upbiter |
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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.