Stryker recalls NICO Myriad Handpieces (NN-8000 to NN-8521) due to latex in packaging that may cause allergic reactions. Consumers should check product numbers and lot numbers for affected items.
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 Handpieces because the packaging tape contains latex, despite being labeled latex-free. This could cause allergic reactions in sensitive individuals. The recall affects specific product models and lot numbers.
The packaging tape for these handpieces contains latex, which is a known allergen. Even though the products are labeled latex-free, the tape used to secure components in the packaging can cause allergic reactions in people with latex sensitivity.
Individuals who own or use the recalled NICO Myriad Handpieces (NN-8000 to NN-8521) are at risk of allergic reactions if they have latex sensitivity. Healthcare professionals using these devices may be affected.
Check the product number on the packaging (NN-8000 to NN-8521) and the lot numbers listed in the recall notice. The affected items include specific model sizes and variants like MHP (Micro Handpiece) and related systems.
Look for the product number (NN-8000 to NN-8521) and lot numbers on the packaging to determine if your item is affected.
The packaging tape contains latex, which can cause allergic reactions in people with latex sensitivity, even though the products are labeled latex-free.
No, the recall does not require stopping use. The issue is with the packaging tape, not the handpieces themselves.
Check the product number (NN-8000 to NN-8521) and lot numbers listed in the recall notice to see if your item is included.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0599-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0599-2026 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.
