Home › SCANLAN INTERNATIONAL INC › SCANLAN® Titanium Forceps
SCANLAN® Titanium Forceps
SCANLAN INTERNATIONAL INC · Model 3003-776 · UDI-DI 00846159003680
GZX
Prescription
10
510(k) clearances
67
Adverse events (1 deaths)
1
Recalls
137
Facilities
Description
S LEG Pus Mic fcp, RH NS DG, 1x2 t, 45° ang 0.5mm DD pft, 8-1/4"/21 cm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-01-22 | Medtronic Xomed, Inc. | A labeling discrepancy was internally identified for the surface electrode component of REF 8263210 AccuGuide EMG Injection Needle, 30G X 25MM. The outside box label correctly ind |
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.