Medline recalls specific valve packs where cannula products may not retain shape. Affected models include DYNJ0415366P and DYNJ0415366Q with certain lot numbers. Consumers should check their kits for these model numbers and lot codes.
The kits contain certain lots of cannula products where the catheter may not retain its shape.
Medline is recalling two specific valve packs (DYNJ0415366P and DYNJ0415366Q) because the cannula products in some lots may not stay shaped properly. This could lead to improper use during medical procedures if the catheter bends or breaks unexpectedly.
The cannula products in certain lots may not retain their shape, which could cause the catheter to bend or break during medical procedures. This might lead to improper placement or complications for patients needing the device.
Healthcare professionals using these valve packs for medical procedures are most at risk. Patients receiving care with affected kits may experience complications if the catheter does not maintain its shape.
Check for model numbers DYNJ0415366P or DYNJ0415366Q on the valve packs. Affected lots include 24DMG366, 25EMD672, 25GMD016, 25AMB610, 25BMJ241, 25CMI425, 24DMC189, 24EMC463, 24GMJ353, and 24IMB824.
Look for model numbers DYNJ0415366P or DYNJ0415366Q on the valve packs.
Confirm the lot number matches the affected lots listed in the recall notice.
The affected models are DYNJ0415366P and DYNJ0415366Q.
Affected lot numbers include 24DMG366, 25EMD672, 25GMD016, 25AMB610, 25BMJ241, 25CMI425, 24DMC189, 24EMC463, 24GMJ353, and 24IMB824.
The recall does not require immediate discontinuation; check the model and lot numbers to determine if your product 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-2670-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2670-2025 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.
