# FDA recall Z-2424-2026

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

## Product

Medline convenience kits:    BASIC  DYNJ905869G    BASIC PACK  DYNJ68484B    BIB GENERAL LAPAROSCOPY PA  DYNJ58305    CHRISTUS CH PEDIATRIC BASIC  DYNJ61167G    CVC INSERTION BUNDLE  CVI3940A    DAVINCI PACK SURGICOUNT  DYNJ45544F    EPCH BASIC PACK  DYNJ83094C    GENERAL PACK  DYNJ39682B  DYNJ84882    GENERAL RFD  DYNJ906336F    GENERAL SURGERY PACK  DYNJT6003    GV MACD PACK  DYNJ46952M    IMPLANT PACK - BBI AR  DYNJ63508A    KIT THORACOSCOPY  DYNJ908872F    LVAD TRAY  DM1120A    MAJOR UROLOGY PACK-LF  DYNJ0368525M    MICRODISECT DECOMPRESS-LF  DYNJ911467    MINOR PACK  DYNJ86972    MULTI PURPOSE PACK  DYNJ58406B    OPEN HEART  DYNJ903245C    P&K PACK  DYNJT5838    PACK,PEDIATRIC MAJOR  DYNJ906888F    PCNL  DYNJ904468C    PEDIATRIC MINOR RFD  DYNJ906296I    PEDIATRIC PACK  DYNJ54239K    PEDIATRIC SURGERY  DYNJ81474B    PERLMUTTER PACK  DYNJT7387    RFT ISC NOBLES MINOR PACK  DYNJ43954B    ROBOTICS FMOL LADY OF THE LAKE  DYNJ89584    ROBOTICS PACK  DYNJ83622B    SCOLI PACK NTX  DYNJ68415C    SMALL ABDOMINAL PACK-LF  PHS41749G    STIM IMPLANT TRIALS  DYNJ87790A    SUPPLEMENTAL PACK  DYNJ65244    TENEX PACK  DYNDH2190    THORACIC PACK  DYNJ56616G    THORACIC PACK SHD  DYNJ68416C    THORACOSCOPY  DYNJ9425843R    THORACOTOMY PM  DYNJ906815A    THORACOTOMY THORACOSCOPY  DYNJ902882D    TRAY,NEONATAL PICC DRSG CHANGE  DYNDC1533B    UNIVERSAL-ASC  DYNJ900071C

## 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-2424-2026
- **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-2424-2026

## Citation

> MORVS. FDA recall Z-2424-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2424-2026. Source: US FDA. Licensed CC0.

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