# FDA recall Z-2436-2026

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

## Product

Medline convenience kits:    ACD  DYNJ904999J    ACDF  DYNJ907336B  DYNJ910821A    ACDF PACK  DYNJ81098C    ACL  DYNJ911996    ACL ACCESSORY PACK  DYNJ86584B    ACL- LF  DYNJ905281B    ACL PACK  DYNJ67271A    ALIF  DYNJ904848L    ANTERIOR CERVICAL  DYNJ901355J    ARTHROSCOPY  DYNJ908193B    ARTHROSCOPY PACK-LF  DYNJ42963M  DYNJ52268B    ARTHROSCOPY SHOULDER  DYNJ908684A    BACK CDS-LF  CDS983364G    BACK PACK  DYNJT4339    CDH SPINE PACK  DYNJ908828D    CERVICAL CDS  DYNJ903477J    CMC ORTHO BACK TRAY  SYNJ10272B    CRANIOTOMY  DYNJ911853    CRANIOTOMY ROOSEVELT PACK  DYNJ58358F    CUSTOM HAND PACK-LF  DYNJ0537135V    CUSTOM SPINAL PACK  DYNJT7544    DISCECTOMY PACK  DYNJ86770    DJ ORTHO SPINE  DYNJ48980M    EXTREMITY PACK-LF  DYNJT4161    FOOT PACK  DYNJ53179D    GENERAL ORTHO-ACNW  DYNJ84891    GILMORE SHOULDER SCOPE PACK  DYNJ58002    GV LUMBAR LAMINECTOMY PK  DYNJ46938L    HAND PACK  DYNJ63113B  DYNJ69662A  DYNJT5855    HAND-LF  DYNJ903263B    KIT LAMINECTOMY  DYNJ908806C    KNEE ARTHROSCOPY  DYNJ902056C  DYNJ904846I    KNEE ARTHROSCOPY-LF  DYNJ905871F    KNEE SCOPE  DYNJ906986G    LAMINECTOMY  DYNJ904847K  DYNJ909505D    LAMINECTOMY CDS  CDS983115K    LAMINECTOMY CERVICAL DISC-LF  DYNJ905286G    LAMINECTOMY NEURO PACK  DYNJ58356F    LAMINECTOMY SPINE  DYNJ904139L    LOWER EXTREMITY PACK  DYNJ63114C    LUMBAR CERVICAL PACK-LF  DYNJ0101088G    LUMBAR LAMI  DYNJ905020J    LUMBAR LAMINECTOMY  DYNJ53707    LUMBAR LAMINECTOMY PACK  DYNJT4386    MAIN/LAMINECTOMY PACK-LF  DYNJ0565499AN    NJ SPINE SPECIALIST PACK  DYNJ58706F    OHOW SPINE-BACK PACK  DYNJ910097A    ORTHO NECK CDS-LF  CDS983134C    ORTHO PACK-LF  DYNJ37202G    ORTHO SPINE  DYNJ40221G    OSC BEACH CHAIR SHOULDER-LF  DYNJ905282C    PACC PETRIE ACL ADD ON PACK-LF  DYNJ58290D    PACK,ARTHROSCOPY ASC  DYNJ65484A    PACK,POSTERIOR SPINAL FUSION  DYNJ906892B    PAD LATERAL SPINE  DYNJ902158L  DYNJ902158M    PAD POSTERIOR SPINE  DYNJ902142L    PK-SPINE  DYNJ58259A    PODIATRY PACK  DYNJ62288D    POST SPINE PACK  DYNJ20509R    POSTERIOR SPINAL FUSION  DYNJ903250B    RFT ARTHROSCOPY PACK  DYNJ43956C    RFT SHOULDER PACK-NOBLE  DYNJ36331D    SA SHOULDER #2 BORDEN  DYNJ56501A    SHOULDER  DYNJ900893M  DYNJ904184I    SHOULDER ARTHROSCOPY  DYNJ904842G    SHOULDER PACK  DYNJ83483    SHOULDER PACK-LF  DYNJ42973N    SHOULDER SCOPE PACK NTX  DYNJ68399C    SPINAL PACK  DYNJ49692G    SPINE  DYNJ910451A    SPINE PACK  DYNJ20147O  DYNJ84971  DYNJ86044A  DYNJ86308C  DYNJ88917  DYNJS3069  DYNJT4163  DYNJT8396    ST CHARLES TOTAL HIP  DYNJ909593C    TOTAL HIP  DYNJ910906D    TOTAL HIP PACK  DYNJ64156B    TOTAL JOINT  DYNJ904186G    TOTAL KNEE PACK  DYNJ60967  DYNJ61409A    WMC ORTHO SPINE WMC-LF  DYNJ902528M    XLIF  DYNJ910795B

## 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-2436-2026
- **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-2436-2026

## Citation

> MORVS. FDA recall Z-2436-2026. Retrieved 2026-10-23 from https://api.morvs.ai/recall/Z-2436-2026. Source: US FDA. Licensed CC0.

---

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