FDA Medical Device Recalls (openFDA)
SVS LLC: PremierPro Aluminum Adjustable Walker
- Recall number
- Z-0487-2019
- Recalling firm
- SVS LLC
- Product
- PremierPro Aluminum Adjustable Walker
- Status
- Terminated
- Initiated
- 2018-10-01
- Posted
- not on file
- Terminated
- 2020-07-13
- Reason
- This recall is due to a mandated order from the FDA for stock recovery and return of the imported item.
- Root cause
- Other
- Action
- SVS LLC, dba S2S Global notified customers initially via telephone on about 10/01/2018 and followed up with a "Notice of Product Recall" letter on about 10/03/2018. The letter requested customers check inventory for affected walkers, quarantine any on hand, make arrangements to return the affected walkers, and complete and return the Medical Device Acknowledgement & Return Response Form.
- Quantity
- 256 devices
- Distribution
- US distribution to OH, NY,TX, PA
- Lot, serial or model codes
- Model 7803. Lot number:: CJH05041. Serial number: J1805000577-J1805000864
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- ITJ
- Firm FEI
- 3007304336
- Firm city
- Charlotte
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28