# FDA recall Z-2431-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-04-27.

## Product

Medline convenience kits:    DAVINCI  DYNJ905836D    DAVINCI-LF  DYNJ905293I    GENERAL ROBOTICS PACK  DYNJT8308    GYN LAP  CDS860087Q    GYN LAPAROSCOPY  DYNJ910084C    GYN LAPAROSCOPY CDS  CDS982371I    GYN LAPAROSCOPY CDS #34-RF  CDS920099S    GYN LAPAROSCOPY PACK  DYNJT3887  DYNJT6876    GYN ROBOTIC CDS  CDS984228K    GYN ROBOTICS  DYNJ911843    KIT LABOR DELIVERY TUBAL LIGAT  DYKMBNDL165C    ROBOTIC LAP CHOLE CDS  CDS985442J    ROBOTIC PACK  DYNJ84725B  DYNJ910594B    ROBOTIC SURGERY PACK  DYNJ53711B    ROBOTICS PACK  DYNJ83622C    UOFL GYN LAPAROSCOPY  DYNJ909322B    WMC ROBOTIC PACK - LF  DYNJ902583O

## Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

## Distribution

US Nationwide distribution. OUS distribution pending.

## Key facts

- **Recall number:** Z-2431-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-27
- **Report date:** 2026-06-24

- **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-2431-2026

## Citation

> MORVS. FDA recall Z-2431-2026. Retrieved 2026-10-17 from https://api.morvs.ai/recall/Z-2431-2026. Source: US FDA. Licensed CC0.

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