LSL Healthcare Infant Central Line Dressing Change Kit Recalled
LSL Healthcare is recalling its Infant Central Line Dressing Change Kit (Model 2925H) distributed nationwide because it contains Webcol Large Alcohol Prep Pads that were recalled for non-sterility.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: This is an FDA Class II recall of a medical device (central line dressing kit) that contains a non-sterile component used in an invasive clinical procedure. Non-sterility in central line dressing kits poses a direct risk of infection in vulnerable populations, particularly infants, meeting the Severe classification for a Class II recall with significant risk of harm.
Plain-English summary
LSL Healthcare Inc. is recalling the Infant Central Line Dressing Change Kit, Model/Catalog Number 2925H. The kit contains Webcol Large Alcohol Prep Pads that were subsequently recalled due to non-sterility concerns.
The recalled kits were distributed nationwide in Maryland, Illinois, and Minnesota. The affected lot number is 6B3022, with an expiration date of November 30, 2026. A total of 220 units were distributed. The product is identified by UDI-DI 00661392052635 and GTIN (01)00661392052635(10)6B3022(17)261130.
Healthcare facilities and individuals who have received this product should discontinue use of the affected dressing change kits immediately. Contact LSL Healthcare Inc. for instructions on proper handling and replacement of the recalled kits.
The recalled product
- Product
- LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H
- Manufacturer
- LSL Healthcare Inc.
- Affected units
- 220
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 (4)
- Lot Code: Model No. 2925H
- UDI-DI 00661392052635
- Lot#6B3022
- Expiration Date 11/30/2026 GTIN: (01)00661392052635(10)6B3022(17)261130
Distribution
Part of a larger recall action
This product is one of 6 recalled by LSL Healthcare Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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