Home › Karl Storz GmbH & Co. KG › D-LIGHT C
D-LIGHT C
Karl Storz GmbH & Co. KG · Model 20133620-134 · UDI-DI 04048551004654
OAY
Prescription
0
510(k) clearances
12
Adverse events
1
Recalls
8
Facilities
Description
Cold Light Fountain D-LIGHT C/US SCB
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. |
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.