Home › ENDO PHARMACEUTICALS INC. › MiniArc
MiniArc
ENDO PHARMACEUTICALS INC. · Model 720191-01 · UDI-DI 00814723020104
PAH
Prescription
10
510(k) clearances
5,966
Adverse events (100 deaths)
1
Recalls
15
Facilities
Description
MiniArc Precise
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-10-26 | Astora | The lot number on the outer carton label did not match the lot number printed on the tray label or identification labels inside the box. The identification labels inside the box a |
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.