Stryker Medical Division of Stryker Corporation: Medical Device Recall in 2023 - (Recall #: Z-0427-2024)

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-400.

Product Classification:

Class II

Date Initiated: August 30, 2023

Date Posted: December 13, 2023

Recall Number: Z-0427-2024

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): 07613327541182. Serial numbers: 2105002838 , 2105002832 , 2202000312 , 2202000286 , 2202000278 , 2202000180 , 2106002241 , 2106001240 , 2107001002 , 2203001053 , 2203001898 , 2112001135 , 2211002054 , 2105002782 , 2210002902 , 2210002890 , 2210002876 , 2210002858 , 2210002848 , 2111001420 , 2206001182

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated