FDA Device recall Z-0487-2019
PremierPro Aluminum Adjustable Walker
- FDA Device
- Class II
- terminated
- Published 2018-11-28
On 2018-11-28 the FDA classified a Class II recall of PremierPro Aluminum Adjustable Walker by Svs, citing this recall is due to a mandated order from the FDA for stock recovery and return of the imported item.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0487-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-10-01 |
| Published | 2018-11-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Svs |
| Distribution | NY, OH, PA, TX |
Product
PremierPro Aluminum Adjustable Walker
Reason
This recall is due to a mandated order from the FDA for stock recovery and return of the imported item.
Identifiers
| code_info | Model 7803. Lot number:: CJH05041. Serial number: J1805000577-J1805000864 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0487-2019%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.