Data Foundry

Medical device recalls 2026

1) UNIVERSAL KIT — Class II medical device recall Z-1330-2026

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 numberZ-1330-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2025-12-24
Classified2026-02-09
Reported by FDA2026-02-18
DistributedNationwide (US)
Quantity21,854 units
Reason classespackaging
UPC / GTIN / UDI-DI10193489388145, 10193489917628, 10198459005848, 10653160289180, 10653160351092, 10653160995340, 10653160996965, 10889942815333, 10889942816453
Lot numbers25EBC706, 25EBC778, 25EBC888, 25EBD964, 25EBE079, 25EBL624, 25EBN178, 25EBN742, 25EBO566, 25EBO757, 25FMI300

Product

1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit SKU DYNDC3107; 8) NON STERILE DIALYSIS KIT, Kit SKU DYNDH1029C; 9) UMBILICAL TRAY W/3.5&5FR CATH, Kit SKU UVT1250; 10) UMBILICAL VESSEL TRAY, Kit SKU UVT835; 11) HEMODIALYSIS TRAY, Kit SKU VAR101HVAA.

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-1330-2026. 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.