ProductGuru Recalls

Official recall record

Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product Description: LIKORALL

US FDA — Medical Devices · 2026-09-14 · United StatesClass II
Issuing authority
US FDA — Medical Devices
Recall initiated by firm
2026-09-14
Country of alert
United States
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
00887761981911
Brand on record
Baxter Healthcare Corporation

What the authority reported

Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quickly than expected during use. Patients are at some risk for injury if a significant fall/drop were to occur due to this issue.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-11-12.

More recalls: US FDA — Medical Devices · United States · all filters

Other recalls from this brand

All 48 official recall notices naming Baxter Healthcare Corporation on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.