FDA Device recall Z-1613-2015
ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch
- FDA Device
- Class II
- terminated
- Published 2015-05-20
On 2015-05-20 the FDA classified a Class II recall of ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch by Handicare Usa, citing complaints were received that the heat-welded seam on the wipeable belt's strap tore when force was applied.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1613-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-26 |
| Published | 2015-05-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Handicare Usa |
| Distribution | CA, FL, MD, NC, NJ |
Product
ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch. Patient transfer aid.
Reason
Complaints were received that the heat-welded seam on the wipeable belt's strap tore when force was applied.
Identifiers
| code_info | All affected product in the U.S are from the same LOT #1402S, Model #s 6133-6136 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1613-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.