Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2023 - (Recall #: Z-0426-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

ProCuity bed series, model number 3009, item number: 3009PX-L-200

Product Classification:

Class II

Date Initiated: August 30, 2023

Date Posted: December 13, 2023

Recall Number: Z-0426-2024

Event ID: 93317

Reason for Recall:

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

Status: Ongoing

Product Quantity:

Code Information:

UDI-DI (GTIN): 07613327541199 Serial numbers: 2211000305 , 2112000828 , 2109001676 , 2109001666 , 2209002657 , 2208001565 , 2208001555 , 2208001541 , 2203002178 , 2203002161 , 2203002159 , 2203002157 , 2106000232 , 2106000210

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated