Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Reported: December 21, 2022 Initiated: November 11, 2022 #Z-0479-2023
Product Description
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.
Details
- Recalling Firm
- Stryker Medical Division of Stryker Corporation
- Units Affected
- 465 (403 US; 62 OUS)
- Distribution
- Worldwide Distribution: US (Nationwide) and Foreign to countries of: Australia, Canada, Netherlands, and United Kingdom.
- Location
- Portage, MI
Frequently Asked Questions
What product was recalled? ▼
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International). Recalled by Stryker Medical Division of Stryker Corporation. Units affected: 465 (403 US; 62 OUS).
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 21, 2022. Severity: Moderate. Recall number: Z-0479-2023.
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