# FDA recall Z-3025-2026

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

## Product

Medline convenience kits labeled as:    1) GYN ROBOTIC CDS, Medline Kit SKU CDS982888Q;   2) GYN ROBOTIC ADD ON PACK, Medline Kit SKU DYNJ43837D;   3) OH GYN/LAP ROBOT PACK, Medline Kit SKU DYNJ89759;   4) GYN LAPAROSCOPY PACK, Medline Kit SKU DYNJ89781;   5) ROBOT ME RF, Medline Kit SKU DYNJ900203N;   6) GYN LAPAROSCOPY, Medline Kit SKU DYNJ900541Q;   7) ROBOTIC, Medline Kit SKU DYNJ903485K;   8) ROBOTIC GYN, Medline Kit SKU DYNJ905230K;   9) LAPAROSCOPIC GYN AND COLON, Medline Kit SKU DYNJ906013I;   10) GYN LAPAROSCOPIC PACK, Medline Kit SKU DYNJ909394B;   11) GYN ROBOTIC, Medline Kit SKU DYNJ909526B;   12) GYN ROBOTIC, Medline Kit SKU DYNJ909526C;   13) GYN ONC ROBOTIC, Medline Kit SKU DYNJ910180;   14) GYN ROBOTIC, Medline Kit SKU DYNJ910181;   15) GYN ROBOTIC, Medline Kit SKU DYNJ910181A;   16) ROBOTICS, Medline Kit SKU DYNJ912062.

## 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-3025-2026
- **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-3025-2026

## Citation

> MORVS. FDA recall Z-3025-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-3025-2026. Source: US FDA. Licensed CC0.

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