Spirit One A-C Powered Hospital Bed
Reported: May 4, 2016 Initiated: July 2, 2015 #Z-1555-2016
Product Description
Spirit One A-C Powered Hospital Bed
Reason for Recall
Customer complaints associated with faulty brake system
Details
- Recalling Firm
- Stryker Medical Division of Stryker Corporation
- Units Affected
- 143 total
- Distribution
- US Distribution to the states of : AL, AZ, FL, GA, HI, IA, IL, KS, LA, MI, MN, MO, NE, NJ, OH, PA, SC, TN and TX., and Internationally to the countries of : Canada and UK.
- Location
- Portage, MI
Frequently Asked Questions
What product was recalled? ▼
Spirit One A-C Powered Hospital Bed. Recalled by Stryker Medical Division of Stryker Corporation. Units affected: 143 total.
Why was this product recalled? ▼
Customer complaints associated with faulty brake system
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 4, 2016. Severity: Moderate. Recall number: Z-1555-2016.
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