Medline recalls specific convenience kits with semi-rigid suction liners made between September 2023 and November 2023 due to potential loss of suction during intermittent use. Affected kits have model MTHZ GYN LAPAROSCOPY and pack numbers DYNJ909739.
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 that could lose suction during intermittent use. This risk may cause incomplete removal of fluids during medical procedures, potentially leading to complications.
The suction liners may lose suction during intermittent use, which can cause incomplete removal of fluids during medical procedures. This could lead to complications if fluids are not properly cleared from the surgical site.
Healthcare professionals using Medline convenience kits with semi-rigid suction liners labeled MTHZ GYN LAPAROSCOPY are most at risk. Patients undergoing procedures with these kits could face incomplete fluid removal.
Check for kits labeled 'MTHZ GYN LAPAROSCOPY' with pack number DYNJ909739. These were manufactured between September 2023 and November 2023 with specific lot numbers: 24BBL055 and 24CBR861.
Look for the label 'MTHZ GYN LAPAROSCOPY' and pack number DYNJ909739 on the kit.
Reach out to Medline Industries for assistance with the recall process.
The recalled suction liners are labeled 'MTHZ GYN LAPAROSCOPY' with pack number DYNJ909739.
These liners were manufactured between September 2023 and November 2023.
Check the kit label for 'MTHZ GYN LAPAROSCOPY' and pack number DYNJ909739. Contact Medline Industries for further assistance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3118-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3118-2024 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.
