Liko Universal Twinbar 670 QRH — Class II medical device recall Z-0829-2022
Ongoing recall by Baxter Healthcare Corporation, reported 2022-04-06, distributed nationwide. An incorrect center bolt was used in the assembly of the product which could result in a patient fall during u
| Recall number | Z-0829-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-02-21 |
| Classified | 2022-03-28 |
| Reported by FDA | 2022-04-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BR, CA, CH, CL, CN, CO, DE, DK, ES, FI, FR, GB, HK, IE, JO, JP, LV, NL, PT, SE, TN, TW, UY, ZA |
| Quantity | 1,399 twinbars |
| UPC / GTIN / UDI-DI | 00887761982468 |
| Model numbers | 3156087, P3156087 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0829-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.