Medline recalls certain kits containing Tego Connectors due to potential silicone seal issues that could cause blood leakage or interrupted therapy. Affected kits include specific SKUs and lot numbers.
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 kits with Tego Connectors that may have damaged silicone seals. This could lead to blood leakage, interrupted therapy, or exposure to contaminants during medical procedures.
Damaged silicone seals in Tego Connectors may cause blood to leak out of the system or air to enter the body. This can interrupt therapy and lead to exposure to contaminants or blood product leakage.
Healthcare professionals using Medline kits for dialysis or blood procedures are most at risk. Patients receiving treatments with these kits could face complications.
Check for the specific SKUs: DYNJ67205C or CVI5200. Look for lot numbers 24BBP627, 24DBO029, 24FBI148, 24JBA858, 24KBD925, 24LBG978, 25ABQ002, 25EBV162, 24EBM915, or 24GBC287.
Identify the lot numbers on the kit packaging to see if they match the affected lots listed in the recall.
Reach out to Medline directly for a replacement kit if the lot numbers match the affected lots.
The affected kits include Medline IR Pack (SKU DYNJ67205C) and Medline NO CATHETER DIALYSIS INSERTION (SKU CVI5200) with specific lot numbers.
The recall states that affected kits may have silicone seal doming or tearing, but there's no specific visual indicator mentioned in the record.
No, the recall does not require immediate stop use; healthcare professionals can continue using the kit but should check lot numbers and contact Medline for a replacement if affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1463-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1463-2026 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.
