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TRICAM®
Karl Storz GmbH & Co. KG · Model 20223020-134 · UDI-DI 04048551350652
OAY
Prescription
0
510(k) clearances
12
Adverse events
1
Recalls
8
Facilities
Description
CCU,TRICAM SL II,USA
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-08-16 | Karl Storz Endoscopy America Inc | The recall was initiated because Karl Storz has confirmed that the Photodynamic Diagnosis (PDD) D-Light C System instruction manuals have important safety-related changes. |
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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.
