Medline recalls apheresis kits containing Tego Connectors due to potential silicone seal doming or tearing, which could cause fluid leaks, therapy interruptions, or exposure to contaminants.
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
Medline is recalling apheresis and central line kits that include Tego Connectors because the silicone seals might dome or tear. This could lead to problems like blood product injection failure, therapy delays, or exposure to biological contaminants.
The silicone seals in Tego Connectors may dome or tear, blocking the fluid path. This can prevent blood product injection or withdrawal with a syringe, causing therapy interruptions, fluid leaks, or exposure to contaminants.
Healthcare professionals using Medline apheresis or central line kits with Tego Connectors are most at risk. Patients receiving treatments through these kits could face complications if the seals fail.
Check for kits with the model numbers DYNDA2705 or DYNJ63347A. The affected lots include specific kit numbers like 24DBL787, 24HBR630, and others listed in the recall notice.
Look for the specific lot numbers listed in the recall notice: 24DBL787, 24HBR630, 25ABH699, 25DBV209, 25GBQ405, 24AMC874, 24AME139, 24AMH820, 24BMF097, 24CMF691, 24GMB769, 24GMK036, 24IMC124, 24LMA110, 25AMJ634, 25GMD386, 25IMB510, 25JMI708.
The silicone seals in Tego Connectors may dome or tear, which can block the fluid path and prevent blood product injection or withdrawal with a syringe.
Check the kit lot numbers listed in the recall: 24DBL787, 24HBR630, 25ABH699, 25DBV209, 25GBQ405, 24AMC874, 24AME139, 24AMH820, 24BMF097, 24CMF691, 24GMB769, 24GMK036, 24IMC124, 24LMA110, 25AMJ634, 25GMD386, 25IMB510, 25JMI708.
No, but you should check the lot numbers to see if your kit is affected. If it is, follow the action steps to ensure safety.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1466-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1466-2026 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.
