FDA Device recall Z-0829-2022
Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087
- FDA Device
- Class II
- ongoing
- Published 2022-04-06
On 2022-04-06 the FDA classified a Class II recall of Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087 by Baxter Healthcare, citing an incorrect center bolt was used in the assembly of the product which could result in a patient fall during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0829-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-02-21 |
| Published | 2022-04-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
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.
Identifiers
| code_info | Manufactured before 28OCT2021, UDI 00887761982468 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0829-2022%22
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