Maryland Heights, MO, United States
Handicare Usa Inc recalls
1 recall recorded since 2018, most recently on 3 November 2017. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 3 November 2017
- Terminated
- 10 July 2020
- Reason
- Premature strap wear and breakage at maximum weight conditions (625 lbs.).
- Distribution
- Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-2752-2018, Z-2753-2018
- Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
- Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.