Dynarex Unna boots and bandages recalled due to temperature exposure between June and August 2021. Product effectiveness may be impacted but not likely to cause health issues.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.
Dynarex Unna boots and bandages from June to August 2021 were recalled because they may have been exposed to higher temperatures during shipping. This could affect product effectiveness but is unlikely to cause health problems.
The products may have been exposed to higher temperatures during shipping from June to August 2021. This could reduce the effectiveness of the dressings but does not pose a risk of serious injury or health problems.
Healthcare facilities that received these products between June 1, 2021 and September 30, 2021 are likely affected. Medical staff using these items for wound care may be at risk if the product was exposed to higher temperatures.
Check for Dynarex Unna boots (3"x10') with catalog #3453 or Unna bandages (4"x10') with catalog #3454 purchased between June 1, 2021 and September 30, 2021.
Verify the product name, size, and catalog number to confirm if it matches the recalled items.
The recall states that the products are unlikely to cause health issues, but effectiveness may be reduced due to temperature exposure.
The recall does not specify a remedy, so contact the manufacturer for guidance on whether to use or dispose of the products.
The recall covers products received between June 1, 2021 and September 30, 2021.
We’ve drafted a message you can send Dynarex to request your refund or repair — edit it as you like.
Subject: Recall Z-1804-2022 — Dynarex Dynarex Hello, I own a Dynarex that is covered by recall Z-1804-2022 from Dynarex. 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.
