# FDA recall Z-3123-2026

> **Medline Industries, LP** · Class I · device recall initiated 2026-08-11.

## Product

Medline Convenience Kits:  1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414;   2) ARTERIAL LINE ST JOES SYR PACK, Catalog Number: DYNJ38145F

## Reason for recall

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-3123-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-08-11
- **Report date:** 2026-09-23

- **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-3123-2026

## Citation

> MORVS. FDA recall Z-3123-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-3123-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*