Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2023 - (Recall #: Z-0428-2024)

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-LE-450.

Product Classification:

Class II

Date Initiated: August 30, 2023

Date Posted: December 13, 2023

Recall Number: Z-0428-2024

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): 07613327541175. Serial numbers: 2109000993 , 2208000147 , 2209000850 , 2211002051 , 2202000910 , 2209000408 , 2205000619 , 2205000615 , 2205000612 , 2205000587 , 2205000746 , 2205000745 , 2205000739 , 2109000135 , 2109000124

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated