# FDA recall Z-1691-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-02-13.

## Product

Medline Kits containing ENFIT G-TUBE CONNECTOR    1. SKU DYKM2720  G/J TUBE CARE KIT    2. SKU ENFITDISCKIT  ENFIT DISCHARGE KIT

## Reason for recall

Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss. Additional consequences may also occur if user over-tightens the connector to stop the leakage, including additional clinical intervention, risk of infection, patient discomfort, and prolonged recovery process.

## Distribution

Worldwide - US Nationwide and the countries of Canada.

## Key facts

- **Recall number:** Z-1691-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-13
- **Report date:** 2026-04-08

- **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-1691-2026

## Citation

> AI Analytics. FDA recall Z-1691-2026. Retrieved 2026-07-07 from https://api.ai-analytics.org/recall/Z-1691-2026. Source: US FDA. Licensed CC0.

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