Handicare Usa Inc: Medical Device Recall in 2018 - (Recall #: Z-2752-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 3, 2017

Date Posted: August 29, 2018

Recall Number: Z-2752-2018

Event ID: 80556

Reason for Recall:

Premature strap wear and breakage at maximum weight conditions (625 lbs.).

Status: Terminated

Product Quantity: 716

Code Information:

Device Model; 323100, 323102, 323117, 323118, 323120, 323137, 323149, 323150, 323215, 323225, 323237, 323240, 323400, 323417, 323450, 323600, 323602, 323700, 323750, 323840, 323851, 323917, 323117V, and 323150V

Distribution Pattern:

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,

Voluntary or Mandated:

Voluntary: Firm initiated