FDA Device recall Z-0503-2015
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities
- FDA Device
- Class II
- terminated
- Published 2014-12-17
On 2014-12-17 the FDA classified a Class II recall of Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities by Snug Seat, citing the bolts, which secure the handles, on the Crocodile (size 3) could break, causing the handle to dislodge.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0503-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-08-26 |
| Published | 2014-12-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Snug Seat |
| Distribution | US |
Product
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The Crocodile is a walking aid for children with disabilities, who need supplementary assistance with their daily walking. The Crocodile is available in three sizes and can be used for children between the ages of 2 to 18 years.
Reason
The bolts, which secure the handles, on the Crocodile (size 3) could break, causing the handle to dislodge.
Identifiers
| code_info | GMDN code; 31119 |
|---|
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-0503-2015%22
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