Medline recalls specific convenience kits with semi-rigid suction liners made between September 2023 and November 2023 due to potential loss of suction during use. Affected kits have labels including MERCY TIFFIN C-SECTION and specific pack numbers.
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
Medline is recalling convenience kits with semi-rigid suction liners made from September to November 2023. These liners may lose suction during intermittent use, which could lead to improper medical suctioning.
The liners may lose suction during intermittent use, meaning they might not function properly when needed. This could lead to inadequate suctioning of medical airways, potentially causing complications.
Healthcare professionals using these kits for medical suctioning are most at risk. Patients receiving suctioning care could be affected if the liners fail.
Check for kits labeled 'MERCY TIFFIN C-SECTION' with pack numbers DYNJ909732. Lot numbers 23LBT911, 24ABX052, or 24CBE496 were produced between September 2023 and November 2023.
Look for the label 'MERCY TIFFIN C-SECTION' and pack number DYNJ909732 on the kit.
Reach out to Medline Industries for specific instructions on how to handle affected kits.
Medline is recalling these kits due to reported adverse events where the suction liners may lose suction during intermittent use.
Check the product labels for the specific pack number and lot numbers mentioned. Contact Medline for further instructions.
The liners may lose suction during intermittent use, which could lead to inadequate suctioning of medical airways.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3119-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3119-2024 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
