Trinity Sterile recalls Wolf-Pak Premium Dressing Kits with GuardVA Cs/30 (Ref: DC5030LF) due to natural rubber latex in packaging. Affected kits may cause allergic reactions in sensitive individuals.
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 Kits with GuardVA Cs/30 (Ref: DC5030LF) because the packaging for component 94-7002 contains natural rubber latex. This poses a risk to people with latex allergies, who could experience allergic reactions.
The packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Individuals with latex allergies could react to this material, potentially causing allergic reactions.
People with latex allergies who use these dressing kits are at risk of allergic reactions. The recall affects specific lot numbers of the Wolf-Pak Premium Dressing Kit with GuardVA Cs/30.
Check for the product name 'Wolf-Pak Premium Dressing Kit with GuardVA Cs/30' and lot numbers 600000-600008 on the packaging. The reference code is DC5030LF.
Look for lot numbers 600000 through 600008 on the packaging of the Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 (Ref: DC5030LF).
No, the recall is for people with latex allergies. If you don't have a latex allergy, there is no risk.
Check the lot numbers on the packaging. If it's 600000-600008, contact Trinity Sterile for guidance.
The recall is for latex allergy risks, not serious injury. The hazard is not severe enough to require immediate action.
We’ve drafted a message you can send Trinity Sterile to request your refund or repair — edit it as you like.
Subject: Recall Z-1549-2022 — Trinity Sterile Trinity Sterile Hello, I own a Trinity Sterile that is covered by recall Z-1549-2022 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.
