SVS LLC recalls PremierPro Aluminum Adjustable Walkers (Model 7805) due to FDA mandated import return. Affected units have specific lot/serial numbers. Consumers should contact SVS for details.
This recall is due to a mandated order from the FDA for stock recovery and return of the imported item.
SVS LLC is recalling PremierPro Aluminum Adjustable Walkers (Model 7803) because of a FDA-mandated order to return imported items. This recall does not involve a safety hazard but is part of a regulatory process for stock recovery.
The recall is due to a FDA-mandated order for stock recovery and return of imported items. There is no safety hazard described in the recall notice. This is a regulatory action, not a safety issue.
Owners of PremierPro Aluminum Adjustable Walkers with lot number CJH05041 or serial numbers J1805000577-J1805000864 are affected. People using these walkers for mobility support may be at risk if they do not return the product.
Check for the model number 7803 on the walker. Look for lot number CJH05041 and serial numbers in the range J1805000577 to J1805000864.
Identify the model number (7803), lot number (CJH05041), and serial numbers (J1805000577-J1805000864) on your walker.
Reach out to SVS LLC for instructions on returning the product as part of the FDA-mandated return process.
This recall is due to a FDA-mandated order for stock recovery and return of imported items, not a safety hazard.
No safety hazard is described in the recall notice. This is a regulatory action for stock recovery.
Check for model number 7803, lot number CJH05041, and serial numbers in the range J1805000577 to J1805000864.
We’ve drafted a message you can send SVS LLC to request your refund or repair — edit it as you like.
Subject: Recall Z-0487-2019 — SVS LLC SVS LLC Hello, I own a SVS LLC that is covered by recall Z-0487-2019 from SVS LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
