Anika Therapeutics recalls Hyalomatrix wound dressings (product numbers 651105, 651103, 651104, 651301) due to potential packaging degradation during sterilization that could compromise product integrity over time.
Hyalomatrix products are susceptible to degradation as a result of the decomposition of PVC in the packaging material during sterilization, which resulted in degradation of the film. Over the long term it is possible that product integrity may be compromised.
Anika Therapeutics is recalling specific Hyalomatrix wound dressings because the packaging material may degrade over time after sterilization, potentially compromising the product's integrity. This could affect the dressing's effectiveness for wound care.
The packaging material contains PVC that can decompose during sterilization, leading to potential degradation of the film over time. This degradation might compromise the product's integrity, though it does not pose an immediate risk to users.
Patients using the recalled Hyalomatrix wound dressings for conditions like wounds, burns, pressure ulcers, or diabetic ulcers are affected. Individuals who have purchased these specific product numbers are most at risk.
Check for product numbers 651105, 651103, 651104, or 651301 on the Hyalomatrix wound dressings. These products were sold with specific batch codes like 2017017A through 2017030A.
Identify if your Hyalomatrix wound dressing has product numbers 651105, 651103, 651104, or 651301.
The packaging material may degrade over time after sterilization, potentially compromising the product's integrity for wound care.
The recall does not specify a remedy, so check the product numbers and contact Anika Therapeutics for further guidance.
The recall indicates potential long-term degradation of the product, but it does not mention immediate risks to users.
We’ve drafted a message you can send Anika Therapeutics to request your refund or repair — edit it as you like.
Subject: Recall Z-2423-2018 — Anika Therapeutics Anika Therapeutics Hello, I own a Anika Therapeutics that is covered by recall Z-2423-2018 from Anika Therapeutics. 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.
