PremierPro Aluminum Adjustable Walker — Class II medical device recall Z-0487-2019
Terminated recall by SVS LLC, reported 2018-11-28, distributed in NY, OH, PA, TX. This recall is due to a mandated order from the FDA for stock recovery and return of the imported item.
| Recall number | Z-0487-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SVS LLC, Charlotte, NC, United States |
| Recall initiated | 2018-10-01 |
| Classified | 2018-11-20 |
| Reported by FDA | 2018-11-28 |
| Terminated | 2020-07-13 |
| Distributed | NY, OH, PA, TX |
| Quantity | 256 devices |
| Lot numbers | CJH05041 |
| Serial numbers | J1805000577-J1805000864 |
| Model numbers | 7803 |
Product
PremierPro Aluminum Adjustable Walker
Reason for recall
This recall is due to a mandated order from the FDA for stock recovery and return of the imported item.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0487-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.