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[Recalled] IMPAK ELASTIC ACRYLIC RESIN POWDER & LIQUID, SHADE TRANSPARENT, CONTENTS: 454 gm Powder + 325ml Liquid, REF 3746, Rx ONLY; Indicated for relining a denture surface — Possible presence of foreign material (rust) | FDA 2016-04-28

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductIMPAK ELASTIC ACRYLIC RESIN POWDER & LIQUID, SHADE TRANSPARENT, CONTENTS: 454 gm Powder + 325ml Liquid, REF 3746, Rx ONLY; Indicated for relining a denture surface
Brand / manufacturerCMP Industries, Llc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2098-2016
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date28 April 2016

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Possible presence of foreign material (rust).

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from CMP Industries, Llc

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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