# FDA recall Z-3020-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-07-10.

## Product

Medline convenience kits labeled as:    1) OPEN HEART PACK, Medline Kit SKU CDS840393P;   2) OPEN HEART PACK, Medline Kit SKU CDS840393Q;   3) OPEN HEART PROCEDURE, Medline Kit SKU CDS980895W;   4) VALVE CDS, Medline Kit SKU CDS981551G;   5) FEM POP, Medline Kit SKU CDS982028W;   6) PACK,OPEN HEART, Medline Kit SKU DYNJ906903F;   7) PACK,CLOSED HEART, Medline Kit SKU DYNJ906904C;   8) ENDOSCOPIC SKULL BASE, Medline Kit SKU DYNJ908362F;   9) OPEN HEART, Medline Kit SKU DYNJ910947;   10) CV, Medline Kit SKU DYNJ911488.

## Reason for recall

Kits contain a potentially contaminated component which were recalled by the manufacturer

## Distribution

US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.

## Key facts

- **Recall number:** Z-3020-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-10
- **Report date:** 2026-09-02

- **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-3020-2026

## Citation

> MORVS. FDA recall Z-3020-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-3020-2026. Source: US FDA. Licensed CC0.

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