Integra LifeSciences recalls CVS Honey Pad models 9370613 and 937404 due to packaging failures that could breach sterile barriers. Affected units include specific lot numbers sold through CVS.
Packaging failures were identified which could lead to a breach in the sterile barrier.
Integra LifeSciences is recalling CVS Honey Pad wound care products with model numbers 9370613 and 937404 because packaging failures might compromise the sterile barrier. This could lead to infection risks for users applying the product to wounds.
The packaging may fail, leading to a breach in the sterile barrier that protects the honey from contamination. This could allow bacteria to enter the wound, increasing infection risk.
People who own or use CVS Honey Pad wound care products with model numbers 9370613 or 937404, particularly those applying the product to wounds. Those with open wounds are at higher risk of infection.
Check for model numbers 9370613 or 937404 on the product. Affected units were sold through CVS with specific lot numbers including 024622, 014622, 044622, and others listed in the recall notice.
Look for model numbers 9370613 or 937404 on the CVS Honey Pad product.
Reach out to CVS customer service for specific lot numbers and instructions on next steps.
The packaging may fail, potentially breaching the sterile barrier and increasing infection risk for users with open wounds.
Check for model numbers 9370613 or 937404. Affected units include specific lot numbers like 024622, 014622, 044622, and others listed in the recall notice.
Contact CVS customer service for specific instructions on how to handle the product, as the recall does not include a direct remedy.
We’ve drafted a message you can send CVS Honey Pad to request your refund or repair — edit it as you like.
Subject: Recall Z-2512-2025 — CVS Honey Pad CVS Honey Pad Hello, I own a CVS Honey Pad that is covered by recall Z-2512-2025 from CVS Honey Pad. 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.
