Data Foundry

Medical device recalls 2026

Medline Kits containing B — Class II medical device recall Z-1060-2026

Ongoing recall by Medline Industries, LP, reported 2026-01-21, distributed nationwide. Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to c

Recall numberZ-1060-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2025-11-26
Classified2026-01-12
Reported by FDA2026-01-21
DistributedNationwide (US)
Quantity338 units
UPC / GTIN / UDI-DI10195327674229, 10198459313745, 10198459364556, 10198459392603, 40195327674220, 40198459313746, 40198459364557, 40198459392604
Lot numbers25HBU964, 25HMC337, 25IBU284, 25IBV819, 25KBF028, 25KBG419, 25KBJ623

Product

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-PLASTIC CRANIOFACIAL PK-LF, Medline kit SKU DYNJ0395085V; 2) NH PERI DISC PACK, Medline kit SKU DYNJ66311C; 3) DISCECTOMY PACK, Medline kit SKU DYNJ86770; 4) TOTAL KNEE, Medline kit SKU DYNJ909643F.

Reason for recall

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

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-1060-2026. 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.