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

Recall Z-0599-2026 — NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NN-8006 11X10 MHP; NN-8007 11x13 MHP; NN-8008 19x28 MHP OI; NN-8010 17x31.5 MHP DECQ; NN-8015

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-0599-2026
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)
00816744028008
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

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