Encore Medical recalls sterile H2O2 products due to mislabeling. Affected items have specific UDI and lot numbers. Consumers should check their product details.
Mislabeling
Encore Medical is recalling sterile hydrogen peroxide products that were mislabeled. This could lead to incorrect use if the product is not properly identified. Consumers should verify their product details to avoid potential misuse.
Mislabeling means the product might not be correctly identified, which could lead to incorrect usage. This is a labeling error rather than a physical defect or hazard in the product itself.
Users of the specific sterile hydrogen peroxide products with the listed UDI and lot numbers are affected. Healthcare professionals and individuals using these products for medical purposes are at higher risk.
Check for the UDI (01)0088891:12108560 and lot number 157N1556 on the product packaging. The product is a sterile hydrogen peroxide solution with specific dimensions (9x38mm).
Look for the UDI (01)00888912108560 and lot number 157N1556 on the product packaging.
The product is a sterile hydrogen peroxide solution with the UDI (01)00888912108560 and lot number 157N1556.
Check for the UDI (01)00888912108560 and lot number 157N1556 on the product packaging.
The recall does not specify a remedy, so check with Encore Medical for further instructions.
We’ve drafted a message you can send Encore Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0626-2024 — Encore Medical Encore Medical Hello, I own a Encore Medical that is covered by recall Z-0626-2024 from Encore Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
