Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2719-2016 — ReliaMed¿ Silver Alginate/CMC. Each dressing is packed in a pouch (primary packaging), each pouch is packed in a carton (secondary packaging) holding multiple (depending on stock keeping unit) pouches and each carton contains one (1) Instructions For Use (IFU) leaflet.

U.S. FDA — Device Enforcement · United Kingdom · 2015-01-15 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2719-2016
Date of alert: 2015-01-15
Country / jurisdiction: United Kingdom
Risk level: Class II
Risk type: recall
Brand: Advanced Medical Solutions Ltd.
Product category: device
Product type: Devices

Reported risk: On 08 January 2015 AMS Sole Customer for the products notified AMS of the issue after discovering the misplaced IFUs during its review of packaging in its warehouse

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-2719-2016 — ReliaMed¿ Silver Alginate/CMC. Each dressing is packed in a pouch (primary packaging), each pouch is packed in a carton (secondary packaging) holding multiple (depending on stock keeping unit) pouches and each carton contains one (1) Instructions For Use (IFU) leaflet.

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