# FDA recall Z-0599-2026

> **Stryker Corporation** · Class II · device recall initiated 2025-10-31.

## Product

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  NICO Fluid System (NFS);  NN-8017  11x13 MHP/PB;  NN-8018  13X13 MHP/PB;  NN-8019  19x28 MHP Little LOTTA;  NN-8020  19x21.5 MHP PaediScope;  NN-8021  15x26.5 MHP LOTTA;      NN-8500  15x10 MHP;  NN-8501  15x13 MHP;  NN-8502  15x25 MINOP MHP;  NN-8503  13x10 MHP;  NN-8504  13x13 MHP;  NN-8505  15x25 GAAB MHP;  NN-8506  11X10 MHP;  NN-8507  11x13 MHP;  NN-8508  19x28 OI MHP;  NN-8510  17x31.5 DECQ MHP;  NN-8517  13X13 MHP/PB;  NN-8518  11x13 MHP/PB;  NN-8519  19x28 Little LOTTA MHP;  NN-8520  19x21.5 PaediScope MHP;  NN-8521  15X26.5 LOTTA MHP;

## Reason for recall

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

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, England, Ireland, Italy, Kuwait, Singapore, Slovenia, Spain, and the Netherlands.

## Key facts

- **Recall number:** Z-0599-2026
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-31
- **Report date:** 2025-12-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portage, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0599-2026

## Citation

> AI Analytics. FDA recall Z-0599-2026. Retrieved 2026-07-25 from https://api.ai-analytics.org/recall/Z-0599-2026. Source: US FDA. Licensed CC0.

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