Medline Soft Suction Canister Liner Recalled for Dimensional Variation
Medline Industries recalls soft suction canister liners due to dimensional variation that may cause difficulty fitting the product into the outer canister. The issue affects units distributed worldwide.
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 for dimensional manufacturing variation affecting product fit and assembly. No illnesses or injuries have been reported. This is a precautionary functional defect recall without explicitly stated patient harm.
Plain-English summary
Medline Industries, LP is recalling soft suction canister liners (1500cc, model DYNDSCL1500) due to a dimensional variation that may cause increased difficulty when fitting the liner into the outer canister.
The affected products were distributed worldwide, including in the United States and internationally to Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, and Singapore.
Users of these products should verify that their units are not affected by checking against the specific lot numbers identified for this recall. Contact Medline Industries, LP with questions about whether a unit is affected.
The recalled product
- Product
- LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500
- Manufacturer
- MEDLINE INDUSTRIES, LP - Northfield
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 (20)
- UDI/DI 40884389129532 (package)
- 10884389129531 (unit)
- Lot Numbers: 670220523
- 670220531
- 670220613
- 670220530
- 670220624
- 670220704
- 670220713
- 670220727
- 670220721
- 670220804
- 670220912
- 670220916
- 670220901
- 670221013
- 670221026
- 670221103
- 670221129
- 670221207
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 21 recalled by MEDLINE INDUSTRIES, LP - Northfield 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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