Stryker recalls NICO BrainPath Shephard's Hook devices with latex in packaging tape. Latex may cause allergic reactions. Affected models include NN-8024, NN-8025, NN-8026, and NN-8042.
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 specific models of NICO BrainPath Shephard's Hook devices because the packaging tape contains latex, despite being labeled latex-free. This could cause allergic reactions in sensitive individuals. The recall affects medical devices used in surgical settings.
The packaging tape contains latex, which can cause allergic reactions in people sensitive to latex. This is a potential hazard because the devices are used in medical settings where patients or staff might come into contact with the tape.
Healthcare professionals and patients using these surgical devices may be affected. Those with latex allergies are at higher risk.
Check for product numbers NN-8024, NN-8025, NN-8026, or NN-8042 on the packaging. The devices are sold with specific lot numbers listed in the recall notice.
Identify the product number and lot numbers from the packaging to confirm if your device is affected.
The packaging tape contains latex, which can cause allergic reactions in people sensitive to latex, despite the devices being labeled latex-free.
Affected models include NICO BrainPath Shephard's Hook with product numbers NN-8024, NN-8025, NN-8026, and NN-8042.
The recall does not require immediate action, but you should check the product details to confirm if your device is affected.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0601-2026 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0601-2026 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.
