# FDA recall Z-2143-2026

> **Medline Industries, LP** · Class I · device recall initiated 2026-03-24.

## Product

Medline medical convenience kits, containing Namic Manifold, Labeled as:    1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C;   2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185;   3. ANGIO KIT, Medline Kit Number/SKUVASC1057.

## Reason for recall

Medline has identified the presence of particulate within the fluid path of the Manifolds.

## Distribution

US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.

## Key facts

- **Recall number:** Z-2143-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-24
- **Report date:** 2026-05-20

- **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-2143-2026

## Citation

> MORVS. FDA recall Z-2143-2026. Retrieved 2026-10-15 from https://api.morvs.ai/recall/Z-2143-2026. Source: US FDA. Licensed CC0.

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