Trinity Sterile recalls Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number 96-1708 due to natural rubber latex in packaging. Those with latex allergies may face risks. Contact for remedy.
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 Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number 96-1708 because the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. This poses a risk to people with latex allergies. The recall is for specific lot numbers and re-order numbers.
The packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. This can cause allergic reactions in people who are sensitive to latex. The risk is specific to those with latex allergies.
People who have the Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number 96-1708 with lot numbers 600001 or 600002 are at risk. Those with latex allergies are most vulnerable.
Check for the re-order number 96-1708 and lot numbers 600001 or 600002 on the Sklar Instruments IV Cath Dressing Tray Cs/25 packaging.
Look for the re-order number 96-1708 and lot numbers 600001 or 600002 on the product packaging.
No, the packaging contains natural rubber latex which can cause allergic reactions in people with latex allergies.
Check the packaging for the re-order number 96-1708 and lot numbers 600001 or 600002. If you have these, contact Trinity Sterile for remedy.
Look for the re-order number 96-1708 and lot numbers 600001 or 600002 on the Sklar Instruments IV Cath Dressing Tray Cs/25 packaging.
We’ve drafted a message you can send Trinity Sterile to request your refund or repair — edit it as you like.
Subject: Recall Z-1548-2022 — Trinity Sterile Trinity Sterile Hello, I own a Trinity Sterile that is covered by recall Z-1548-2022 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.
