Home › Karl Storz GmbH & Co. KG › n.a.
n.a.
Karl Storz GmbH & Co. KG · Model 496U · UDI-DI 04048551169629
FCS
Prescription
10
510(k) clearances
93
Adverse events
3
Recalls
13
Facilities
Description
Fiber Optic Ureter Probe
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-07 | Cook Inc. | Product may overheat, melt, and burn patient. |
| 2008-05-09 | Stryker Endoscopy | Kit fibers may not illuminate along entire length, which may result in inadequate visibility of the urethral structures during surgery |
| 2008-05-09 | Stryker Endoscopy | Kit fibers may not illuminate along entire length, which may result in inadequate visibility of the urethral structures during surgery |
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.