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Serious recall: Injury is possible or has been reported. Take action promptly.

Medline Industries, LP 2026-03-04 Health serious FDA
Health · FDA · Recall #FDA-Z-1468-2026

Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167 Recall

Issued March 4, 2026 · Medline Industries, LP

In March 2026, Medline Industries, LP recalled the Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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.

What you should do

  1. 1 Stop using Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167 right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Medline Industries, LP to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Medline Industries, LP
Category
Health
Recall date
March 4, 2026
Units affected
Not reported
Sold at
US Nationwide distribution.
Recall number
FDA-Z-1468-2026
Made in
United States
Issuing agency
FDA

In context

  • Medline Industries, LP has 50 recalls in our database, including 8 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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