Medline abdominal and bariatric packs contain recalled Mastisol liquid adhesive
Medline convenience kits including abdominal, bariatric and laparoscopic cholecystectomy packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
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: FDA Class II recall where the described consequence is that a component becomes unusable rather than any patient hazard, which fits the Moderate band.
Plain-English summary
Medline convenience kits are being recalled, covering the ABD Pack (DYNJ81673B), Bariatric (DYNJ902515K), Bariatric + (DYNJ904119O), Bariatric CDS (CDS983883J), the BWNBORO Lap Chole Pack-LF (DYNJ32836B) and the CCSB Karin JWire Lumpectomy kit (DYNJ910459B), among the SKUs listed in the recall notice. The action covers 49,654 kits in total across the connected Medline Mastisol recalls.
The stated reason is that the kits contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive. According to the notice, the butyrate tubing may crack during actuation and render the product unusable for application. The FDA classified the action as Class II. The source does not describe any patient hazard beyond the product being unusable.
Distribution was nationwide in the United States, with distribution outside the United States pending.
Facilities should identify affected stock using the kit numbers, UDI-DI codes and lot numbers in the recall notice and follow the instructions issued by Medline.
The recalled product
- Product
- Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS CDS983883J BWNBORO LAP CHOLE PACK-LF DYNJ32836B CCSB KARIN JWIRE LUMPECTOMY DYNJ910459B CHRISTUS CHILDRENS LAP CHOLE DYNJ61165G CUH MINOR PACK-
- Manufacturer
- Medline Industries, LP
- Affected units
- 49,654
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 34 recalled by Medline Industries, LP 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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