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Terminated

Carepak Sheer Adhesive Bandages 50 Sterile Bandages Assorted Sizes

FDA Recall Z-2460-2015 · Posted 2015-08-25

Recalling FirmASO, LLC
Recall StatusTerminated
Product CodeKGX
Date Initiated2015-06-10
Date Terminated2016-10-12
Product Quantity655 cases.

Reason for Recall

Contain 0.1% Benzalkonium Chloride in the 5/8 bandages inside the assortment which is not listed as an active ingredient in the product label.

Firm Action

Customers were contacted by phone and e-mail on 06/10/2015; First class letter was sent on 06/23/2015.

Root Cause

Process control

Distribution Pattern

US Distribution to Rhode Island only

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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