PlainRecalls
FDA Devices Moderate Class II Ongoing

ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.

Reported: December 13, 2023 Initiated: August 30, 2023 #Z-0432-2024

Product Description

ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.

Reason for Recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Details

Distribution
Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
Location
Portage, MI

Frequently Asked Questions

What product was recalled?
ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.. Recalled by Stryker Medical Division of Stryker Corporation.
Why was this product recalled?
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 13, 2023. Severity: Moderate. Recall number: Z-0432-2024.