Recall Z-0820-2022— Baxter Healthcare Corporation

Name: FDA recall Z-0820-2022
Creator: U.S. Food and Drug Administration
Published: 2022-02-14

Class II · Ongoing

Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2022-02-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Compella Bariatric Bed System. Reason: Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains..

Recalling firm: Baxter Healthcare Corporation
Classification: Class II
Status: Ongoing
Initiated: 2022-02-14
Firm location: Deerfield, IL, United States

Product description

Compella Bariatric Bed System

Reason for recall

Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.

Data sourced from openFDA. This site is unofficial and independent of the FDA.