Medline recalls dental suction kits with specific pack numbers from September to November 2023 due to potential loss of suction during intermittent use. Affected kits may require replacement to prevent incomplete suction.
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 dental suction kits with pack number DYNJ909451A made between September and November 2023. These kits might lose suction during intermittent use, which could lead to incomplete removal of fluids during dental procedures.
The suction liners in these kits may lose suction during intermittent use, meaning they might not effectively remove fluids from the mouth. This could lead to incomplete suction during dental procedures, potentially causing fluid buildup or discomfort.
Dental professionals using Medline convenience kits with the specific pack number DYNJ909451A manufactured between September and November 2023 are most at risk. Patients receiving dental care with these kits may also be affected.
Check for the pack number DYNJ909451A on the kit label. The kits were manufactured between September 2023 and November 2023 with lot number 23LMI232.
Look for the pack number DYNJ909451A on the kit label to confirm if it is affected.
Reach out to Medline Industries for replacement or further instructions if the kit is affected.
The affected kits have pack number DYNJ909451A.
These kits were manufactured from September 2023 to November 2023.
Contact Medline Industries for replacement or further instructions if the kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3108-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3108-2024 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.
