Home › AMERICAN DIAGNOSTIC CORP › Metalite™
Metalite™
AMERICAN DIAGNOSTIC CORP · Model 352WQ · UDI-DI 00634782062736
6
510(k) clearances
10
Adverse events
1
Recalls
159
Facilities
Description
METALITE Penlight,White, Disp pkg
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-03-20 | DermLite LLC | Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling. |
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.