Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.
Check against the official notice below — it lists the full affected range.
Baxter Healthcare Corporation is recalling the Liko Universal Twinbar 670 QRH (model numbers 3156087 and P3156087), an accessory used with most Liko lifts. The recall affects 1,399 units manufactured before October 28, 2021. An incorrect center bolt was used during assembly of these products, which could cause a patient to fall during use.
The recalled twinbars were distributed worldwide, including nationwide distribution across numerous U.S. states and multiple countries including Canada, Australia, Brazil, China, and various European nations. The source document does not specify a remedy or what affected consumers should do.
Written by software from the official notice below. Not reviewed by a lawyer.
An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use.
Reason for recall: An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use. 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 distribution but no military distribution. The countries of Austria, Australia, Brazil, Canada, Chile, China, Colombia, Denmark, Finland, France, Germany, Hong Kong, Irel Quantity: 1,399 twinbars Lot/code info: Manufactured before 28OCT2021, UDI 00887761982468
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.