ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.
Reported: December 13, 2023 Initiated: August 30, 2023 #Z-0435-2024
Product Description
ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.
Reason for Recall
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Details
- Recalling Firm
- Stryker Medical Division of Stryker Corporation
- 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? ▼
ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.. 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-0435-2024.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11