Stryker recalls NICO Myriad Illumination Packs (NN-1000/NN-1001) due to latex in packaging that may cause allergic reactions. Affected units include specific product numbers and lot codes.
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
Stryker is recalling NICO Myriad Illumination Packs (NN-1000 and NN-1001) because the packaging tape contains latex, which could cause allergic reactions in sensitive individuals. This is a safety concern for people with latex allergies who might react to the tape.
The packaging tape for these products contains latex, even though the products are labeled as latex-free. Latex can cause allergic reactions in sensitive individuals, which may lead to symptoms like skin irritation, swelling, or more severe reactions in rare cases.
People who own or use the NICO Myriad Illumination Packs (NN-1000 and NN-1001) are affected. Those with latex allergies are at higher risk of an allergic reaction.
Check for product numbers NN-1000 or NN-1001 on the packaging. Affected units have specific lot codes listed in the recall notice, including sequences like 37AC5163 and 37AE9811.
Look for product numbers NN-1000 or NN-1001 on the packaging to confirm if your item is affected.
The packaging tape contains latex, which can cause allergic reactions in sensitive individuals, even though the products are labeled as latex-free.
No, the recall is for the packaging tape, not the products themselves. You can continue using the products if you don't have latex allergies.
Check for product numbers NN-1000 or NN-1001 and specific lot codes listed in the recall notice, such as 37AC5163 or 37AE9811.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0600-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0600-2026 from Stryker. 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.
