Recall Z-0829-2022— Baxter Healthcare Corporation
Class II · Ongoing
Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2022-02-21. FDA's recall record names no specific 510(k) clearance for this event. Product: Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.. Reason: An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use..
- Recalling firm
- Baxter Healthcare Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-02-21
- Firm location
- Deerfield, IL, United States
Product description
Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.
Reason for recall
An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use.
Data sourced from openFDA. This site is unofficial and independent of the FDA.