Data Foundry

Medical device recalls 2026

Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage… — Class II medical device recall Z-1562-2026

Ongoing recall by Medline Industries, LP, reported 2026-03-18, distributed nationwide. The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have

Recall numberZ-1562-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-01-30
Classified2026-03-12
Reported by FDA2026-03-18
DistributedNationwide (US)
Countries outside the USCL, PA
Quantity2,894 units
UPC / GTIN / UDI-DI10193489496635, 10193489980110, 10198459155895, 40193489496636, 40193489980111, 40198459155896
Lot numbers21HMB801, 21HMG569, 21IMG797, 22FMA481, 22KBO714, 22KMG297, 23DBC954, 23DBJ852, 23FBF593, 23GBE709, 23GBE710, 23HBU475, 23IBQ646, 23JBJ077, 23JBP214, 24ABN040, 24BBA256, 24BBP532, 24FBS256, 24GBC436, 24HBM020, 24LBJ019, 25ABA001, 25DBB810, 25EBP586, 25EBP587, 25EBP588, 25EBP589, 25EBP602, 25EBT976, 25FBO822, 25GBA989, 25GBK350, 25HBF488, 25HBH137, 25HBO806, 25HBT069, 25IBK435, 25JBG183, 25JBN467 and 2 more
Model numbersDYNJ902487A, DYNJ908126, DYNJ910851

Product

Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Number: DYNJ908126; 3) CARDIO CONGENITO, Model Number: DYNJ910851

Reason for recall

The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.

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-1562-2026. 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.