# FDA recall Z-1467-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-01-08.

## Product

Convenience kits containing Tego Connectors:    Medline DIALYSIS DRESSING CHANGE  SKU EBSI1498    Medline DIALYSIS DRESSING CHANGE KIT  SKU EBSI1107  EBSI1596  EBSI1781  EBSI1812    Centurion DIALYSIS/PHERESUS CVC DRSG CHANGE KIT  SKU DT22630    Medline DIALYSIS/PHERESIS DRESSING CHANGE KIT  SKU EBSI1470    Centurion VASCATH DRESSING CHANGE TRAY  SKU DT22845

## Reason for recall

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.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1467-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-08
- **Report date:** 2026-03-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1467-2026

## Citation

> AI Analytics. FDA recall Z-1467-2026. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1467-2026. Source: US FDA. Licensed CC0.

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