Use cautionMedical device recall · FDA · Published February 21, 2022
Baxter Healthcare Liko Universal Twinbar 670 QRH Recall: Risk of Patient Fall
Baxter Healthcare recalls Liko Universal Twinbar 670 QRH lifts with incorrect center bolt that could cause patient falls. Model numbers 3156087 and P3156087, manufactured before October 28, 2021.
“Baxter Healthcare Liko Universal Twinbar 670 QRH Recall: Risk of Patient Fall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61125-baxter-healthcare-liko-universal-twinbar-670-qrh-recall-risk-of. Based on FDA recall #Z-0829-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0829-2022%22&limit=1).
Baxter Healthcare Corporation recalled Liko Universal Twinbar 670 QRH lift accessories due to an incorrect center bolt that could cause patient falls, according to the FDA on Feb. 21, 2022.
How to tell if you have it
Brand: Baxter Healthcare
Product: Liko Universal Twinbar 670 QRH
Model numbers: 3156087 and P3156087
Manufactured before 28OCT2021
UDI: 00887761982468
The hazard
An incorrect center bolt was used in the assembly of the product, which could result in a patient fall during use.
Context
GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since Sept. 2, 2015. Other recent recalls of similar products include Molift 4-Point Sling Bars Recall (Nov. 17, 2025) and Genesis Screw-In Anchor Recall (Dec. 17, 2025).
How to tell if you have this one
Check for model numbers 3156087 or P3156087 on the product. These lift accessories were manufactured before October 28, 2021, and have a unique device identifier (UDI) starting with 00887761982468.
Brand
Baxter Healthcare
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Model
Look for model numbers 3156087 or P3156087 on the product label.
Contact Manufacturer
Reach out to Baxter Healthcare for guidance on next steps if you have the recalled product.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 33 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of AK, AZ, CA, CO, DC, FL, GA, HI, IA, ID, IN, KS, KY, LA, MA, MD, MI, MN, MO, ND, NE, NJ, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, and WI. There was government…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alaska, Arizona, California, Colorado, District of Columbia, Florida, Georgia, Hawaii, Idaho, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Nebraska, Nevada, New Jersey, New York, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin.
Recall timeline
FDA published this recall 44 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0829-2022 (February 21, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0829-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.