Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0601-2026 — NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;

U.S. FDA — Device Enforcement · United States · 2025-10-31 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0601-2026
Date of alert: 2025-10-31
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00816744028244

Reported risk: Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0601-2026 — NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;

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