ProCuity bed series, model number 3009, item number: 3009PX-L-200
FDA Recall #Z-0426-2024 — Class II — August 30, 2023
Product Description
ProCuity bed series, model number 3009, item number: 3009PX-L-200
Reason for Recall
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Recalling Firm
Stryker Medical Division of Stryker Corporation — Portage, MI
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Distribution
Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
Code Information
UDI-DI (GTIN): 07613327541199 Serial numbers: 2211000305 , 2112000828 , 2109001676 , 2109001666 , 2209002657 , 2208001565 , 2208001555 , 2208001541 , 2203002178 , 2203002161 , 2203002159 , 2203002157 , 2106000232 , 2106000210
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated