PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: May 13, 2020 Initiated: January 7, 2020 #Z-1925-2020

Product Description

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.

Details

Recalling Firm
Stryker Corporation
Units Affected
26,298 units
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.
Location
San Jose, CA

Frequently Asked Questions

What product was recalled?
Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only sold in the US. Drape/ UDI: HH2000/10858701006329; HH9006/ 10858701006282. Recalled by Stryker Corporation. Units affected: 26,298 units.
Why was this product recalled?
Sterile drapes packaged in an unsealed pouch.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 13, 2020. Severity: Moderate. Recall number: Z-1925-2020.