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

FDA Recall #Z-1256-2023 — Class II — February 1, 2023

Recall #Z-1256-2023 Date: February 1, 2023 Classification: Class II Status: Ongoing

Product Description

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.

Recalling Firm

Stryker Medical Division of Stryker Corporation — Portage, MI

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

4 units

Distribution

US Nationwide distribution in the states of NY, VA.

Code Information

GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

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