MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
FDA Recall Z-0696-2022 · Posted 2022-03-01
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Recalling FirmMEDLINE INDUSTRIES, LP - Northfield
Recall StatusOpen, Classified
Product CodeLRJ
Date Initiated2021-12-29
Product Quantity359,524 units
Reason for Recall
Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.
Firm Action
The firm initiated the recall on January 13, 2022 and provided each consignee with a letter and a response form to record their response to the recall notification. Each response received will be recorded and the firm will send subsequent letters to consignees that have not provided a response to the recall notification in the allotted time. The letter explained the issue and requested return of the product, if available. Customers will be responsible for initiating sub-recall procedures. Any recalled product that is returned from customers will be quarantined at the firm's corporate office pending destruction.
The firm expanded the original recall notification dated January 13, 2022 to include additional lots of the Micro-Kill Bleach Germicidal Bleach Wipes due to product not meeting label claim for Sodium Hypochlorite content. A letter was sent out to all consignees within the scope of the expanded recall on 02/25/2022 with the same instructions.
The firm sent a letter dated July 27, 2022, to previous non-responding consignees instructing them to destroy any affected product per their local and state regulations and document the destruction.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Panama and Bermuda.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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