FDA recall Z-1256-2023

Stryker Medical Division of Stryker Corporation · Class II · device

Product

Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001

Reason for recall

Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.

Distribution

US Nationwide distribution in the states of NY, VA.

Key facts

Status
Ongoing
Initiation date
2023-02-01
Report date
2023-03-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Portage, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1256-2023