Handicare USA, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1613-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch. Patient transfer aid.

Product Classification:

Class II

Date Initiated: March 26, 2015

Date Posted: May 20, 2015

Recall Number: Z-1613-2015

Event ID: 70995

Reason for Recall:

Complaints were received that the heat-welded seam on the wipeable belt's strap tore when force was applied.

Status: Terminated

Product Quantity: 64

Code Information:

All affected product in the U.S are from the same LOT #1402S, Model #s 6133-6136

Distribution Pattern:

US Distribution to the states of : FL, CA, NJ, NC and MD.

Voluntary or Mandated:

Voluntary: Firm initiated