FDA recall Z-0479-2023

Stryker Medical Division of Stryker Corporation · Class II · device

Product

Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)

Reason for recall

Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.

Distribution

Worldwide Distribution: US (Nationwide) and Foreign to countries of: Australia, Canada, Netherlands, and United Kingdom.

Key facts

Status: Ongoing
Initiation date: 2022-11-11
Report date: 2022-12-21
Voluntary/Mandated: Voluntary: Firm initiated
Location: Portage, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0479-2023