Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE… — Class II medical device recall Z-1334-2026
Ongoing recall by Medline Industries, LP, reported 2026-02-18, distributed nationwide. Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPre
| Recall number | Z-1334-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-12-24 |
| Classified | 2026-02-09 |
| Reported by FDA | 2026-02-18 |
| Distributed | Nationwide (US) |
| Quantity | 8,445 kits |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10193489499247, 10195327475482, 10198459078880, 10653160259268, 10653160283041, 10653160283263, 10653160320593, 10653160323303, 10653160997504 |
| Lot numbers | 25EBC730, 25EBD629, 25EBH827, 25EBI085, 25EBM451, 25EBQ881, 25EBU086, 25EMJ081, 25EMJ351 |
Product
Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESSING CHANGE K, Kit SKU DT19665; 6) NEONATAL DRESSING CHANGE KIT, Kit SKU DT21495; 7) NICU CVC DRESSING CHANGE TRAY, Kit SKU DT22510A; 8) DRESSING CHANGE TRAY W/TEG CHG, Kit SKU DYNDC3114B; 9) DRESSING CHANGE KIT, Kit SKU DYNDC3351.
Reason for recall
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
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-1334-2026. 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.