Trinity Sterile recalls Wolf Pak Premium Dressing Change Kits with natural rubber latex in packaging. Risk of allergic reaction for sensitive users. Check lot numbers 600000-600019.
Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy
Trinity Sterile is recalling Wolf Pak Premium Dressing Change Kits that contain natural rubber latex in packaging. This poses a risk of allergic reactions for people with latex allergies. Affected kits have specific lot numbers listed in the recall.
The packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. This can cause allergic reactions in individuals sensitive to latex. The kits are labeled as latex-free but contain latex in the packaging.
People who use these dressing kits, especially those with latex allergies, are at risk. The recall affects users of the Wolf Pak Premium Dressing Change Kit with specific lot numbers.
Check the lot numbers on the packaging: 600000 through 600019. The product is the Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Cs/30, reference DC5090LF.
Look for lot numbers 600000 to 600019 on the packaging of the Wolf Pak Premium Dressing Change Kit.
Yes, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex.
People with latex allergies may experience allergic reactions due to the natural rubber latex in the packaging.
Check the lot numbers on the packaging: 600000 through 600019 for the Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Cs/30, reference DC5090LF.
We’ve drafted a message you can send Trinity Sterile to request your refund or repair — edit it as you like.
Subject: Recall Z-1551-2022 — Trinity Sterile Trinity Sterile Hello, I own a Trinity Sterile that is covered by recall Z-1551-2022 from Trinity Sterile. 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.
