Hill-Rom recalls LikoStretch 1900 Model 3156051 due to potential patient sliding and falling during lifts. Affected users should contact Hill-Rom for details.
Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.
Hill-Rom is recalling the LikoStretch 1900 model 3156051 because it can lose its ability to keep patients horizontal during lifts, causing them to slide backward and potentially fall. This poses a risk of injury to patients during medical procedures.
The stretch leveller may stop working properly when lifting a patient, causing them to slide backward. If the patient falls out of the lift sheet, they could hit the surface they're being lifted from, leading to injury.
Healthcare workers using the LikoStretch 1900 for patient lifts are most at risk. Patients being moved with this device could slide and fall if the stretch leveller malfunctions.
Check for the LikoStretch 1900 model number 3156051. This product was sold for patient lifts in healthcare settings.
Reach out to Hill-Rom directly for instructions on how to handle the recalled product.
Yes, the stretch leveller may lose its ability to keep patients horizontal during lifts, causing them to slide backward and potentially fall.
Look for the LikoStretch 1900 model number 3156051, which was sold for patient lifts in healthcare settings.
Contact Hill-Rom directly for instructions on how to handle the recalled product.
We’ve drafted a message you can send Hill-Rom to request your refund or repair — edit it as you like.
Subject: Recall Z-2600-2021 — Hill-Rom Hill-Rom Hello, I own a Hill-Rom that is covered by recall Z-2600-2021 from Hill-Rom. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
