FDA recall Z-2753-2018

Product

Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

Reason for recall

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,

Key facts

Status

Terminated

Initiation date

2017-11-03

Report date

2018-08-29

Termination date

2020-07-10

Voluntary/Mandated

Voluntary: Firm initiated

Location

Maryland Heights, MO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2753-2018