# FDA recall Z-2423-2026

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

## Product

Medline convenience kits:    BREAST IMAGING  DYNJT5893    CHOG PLASTICS  SYNJ10306A    ENDO BREAST AUGMENTATION PACK  DYNJ68023    FACIAL PLASTIC  DYNJ909926C    JVL - MODULE PLASTIC PK  DYNJ84081B    KIT MAJOR PLASTICS MOSES  DYNJ905362C    MEM MAXILLOFACIAL PACK-LF  DYNJ0660040R    MINOR BREAST PACK  DYNJ89023A    PLASTIC MAJOR SURGERY  DYNJ902510M    PLASTIC PACK  DYNJ84766    PLASTIC PACK-LF  DYNJ0578842M    PLASTICS EXTREMITY PACK  DYNJ63803C    PLASTICS PK - NO SYR  DYNJ62433D    RR-ASC-RHINOPLASTY PACK-LF  DYNJ81772C    TRANSGENDER PACK  DYNJT7588    WH PLASTIC MAJOR PACK  DYNJ89048A

## 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-2423-2026
- **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-2423-2026

## Citation

> MORVS. FDA recall Z-2423-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2423-2026. Source: US FDA. Licensed CC0.

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