Data Foundry

Medical device recalls 2026

Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS… — Class II medical device recall Z-2423-2026

Ongoing recall by Medline Industries, LP, reported 2026-06-24, distributed nationwide. Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during

Recall numberZ-2423-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-04-27
Classified2026-06-12
Reported by FDA2026-06-24
DistributedNationwide (US)
Quantity49,654 kits
Reason classespackaging
UPC / GTIN / UDI-DI10193489288292, 10193489296891, 10193489468083, 10195327414108, 10198459149825, 10198459346842, 10198459349362, 10198459388316, 10198459388477, 10198459423109, 10198459462474, 10198459498176, 10198459517839, 10198459635182, 10198459683374, 10889942220083
Lot numbers25JME572, 25KBA123, 25KBC500, 25KBC752, 25KBI169, 25KBM917, 25KBN239, 25LBC067, 25LBF694, 25LBN476, 25LBO305, 25LBR659, 25LMG027, 25LMH594, 25LMI396, 25LMI881, 26AMA250, 26AMA936, 26BBC049, 26BBD124, 26CBC156, 26CBD081, 26CBM279, 26CBO942, DYNJ0578842M, DYNJ0660040R, DYNJ62433D, DYNJ63803C, DYNJ68023, DYNJ81772C, DYNJ84081B, DYNJ84766, DYNJ89023A, DYNJ89048A, DYNJ902510M, DYNJ905362C, DYNJ909926C, DYNJT7588, SYNJ10306A

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2423-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.