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NEODERM

Conmed Corporation · Model 745-1000 · UDI-DI 10653405014591

MGP Prescription
10
510(k) clearances
95
Adverse events (1 deaths)
1
Recalls
22
Facilities

Description

NeoDerm Plus Transparent Membrane Dressing with Adhesive Border

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

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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.