# FDA recall Z-1925-2020

> **Stryker Corporation** · Class II · device recall initiated 2020-01-07.

## Product

Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only sold in the US.  Drape/ UDI: HH2000/10858701006329;   HH9006/ 10858701006282

## Reason for recall

Sterile drapes packaged in an unsealed pouch.

## Distribution

US - Nationwide &  Puerto Rico  OUS - Netherlands, Spain, Switzerland, Colombia, Canada, Japan, Taiwan, Puerto Rico, South Africa, South Korea, Australia, Chile, China, Germany, France, United Kingdom, Hong Kong, India, Italy, Singapore, Thailand, Romania, Belgium, Sweden, Switzerland, Austria, Malaysia, Finland, Denmark, Israel, Qatar, Kazakhstan, Turkey, Czech Republic, Greece, Russia, Poland, Ireland,  Philippines, and New Zealand.

## Key facts

- **Recall number:** Z-1925-2020
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-01-07
- **Report date:** 2020-05-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Jose, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1925-2020

## Citation

> AI Analytics. FDA recall Z-1925-2020. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/Z-1925-2020. Source: US FDA. Licensed CC0.

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