FDA Mandates Recall of PremierPro Aluminum Adjustable Walkers
SVS LLC is recalling 256 PremierPro Aluminum Adjustable Walkers due to an FDA order for stock recovery and return of imported items.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is an FDA Class II mandated stock recovery with no reported injuries or specific safety defects cited in the source text, fitting the criteria for a moderate, precautionary administrative action.
Plain-English summary
SVS LLC is recalling 256 units of the PremierPro Aluminum Adjustable Walker (Model 7803) in response to a mandated order from the U.S. Food and Drug Administration. The recall involves the stock recovery and return of the imported item.
The affected devices are identified by Lot number CJH05041 and Serial numbers ranging from J1805000577 to J1805000864. These products were distributed in the United States to Ohio, New York, Texas, and Pennsylvania.
Consumers who possess this product should stop using it and contact SVS LLC for instructions on returning the device as part of the stock recovery process.
The recalled product
- Product
- PremierPro Aluminum Adjustable Walker
- Manufacturer
- SVS LLC
- Category
- Medical Device — Mobility Aids
- Hazard
- Affected units
- 256
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Model 7803. Lot number:: CJH05041. Serial number: J1805000577-J1805000864
Distribution
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