FDA Device Intelligence
HomeSMITH & NEPHEW MEDICAL LIMITED › ACTICOAT 3 5" X 5"

ACTICOAT 3 5" X 5"

SMITH & NEPHEW MEDICAL LIMITED · Model 20151 · UDI-DI 00040565122045

MGP Prescription
1
510(k) clearances
95
Adverse events (1 deaths)
1
Recalls
22
Facilities

Description

Silver-coated antimicrobial barrier dressing

Recalls

DateFirmReason
2011-02-11Hartmann USA, IncMisbranded; the expiry date on the primary packing incorrectly indicates 2010-10, instead of 2015-10. Consignees were notified by letter on/about 02/11/2011. They were advised to e

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 docs
Data 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.