Medline Recalls Semi-Rigid Suction Liners Due to Suction Loss
Medline Industries is recalling 19 units of semi-rigid suction liners due to reported adverse events involving potential loss of suction during use.
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: The source text explicitly states the recall is due to 'reported adverse events.' Per the rubric, FDA Class II recalls with reported adverse events (implying injury or significant risk) are classified as Severe (Score 4).
Plain-English summary
Medline Industries, LP is recalling 19 units of 1500 cc semi-rigid suction liners. The affected products are Medline convenience kits labeled 'DENTAL' with Pack Number DYNJ909451A and Lot Number 23LMI232. These units were manufactured between September 2023 and November 2023.
The recall is being issued due to reported adverse events. The specific hazard is the potential loss of suction or low suction during intermittent suction use. The agency has classified this as a Class II recall.
The affected products were distributed worldwide, including the United States, Canada, and Panama. Users should stop using the affected liners and contact Medline Industries for further instructions.
The recalled product
- Product
- Medline convenience kits containing semi-rigid suction liners labeled as follows: DENTAL, Pack Number DYNJ909451A
- Manufacturer
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Medical Device — Suction Liners
- Affected units
- 19
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)
- DYNJ909451A
- UDI/DI case 40195327478392
- UDI/DI each 10195327478391
- Lot Numbers: 23LMI232
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 17 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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