CADD-Solis Li-ion Rechargeable Battery Packs recall
CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160-XX, which are also sold as a component of the following CADD Solis Ambulatory Infusion…
Why was CADD-Solis Li-ion Rechargeable Battery Packs recalled?
Damage to the battery pack may have caused a short to a capacitor within the battery pack. While the battery encasement is designed to be flame retardant, a short to the capacitor could lead to melting of the battery pack case. If this issue occurs, the battery pack charging circuit may become inoperable.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All serial numbers.
- Product
- CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160-XX, which are also sold as a component of the following CADD Solis Ambulatory Infusion…
- Recalling firm
- Smiths Medical ASD Inc.
- Quantity
- 138039 units
- Distribution
- Worldwide Distribution
- Recall date
- November 6, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)