Data Foundry

Medical device recalls 2026

Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB — Class II medical device recall Z-1833-2026

Ongoing recall by Medline Industries, LP, reported 2026-04-29, distributed nationwide. The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have be

Recall numberZ-1833-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-02-25
Classified2026-04-17
Reported by FDA2026-04-29
DistributedNationwide (US)
Quantity58,836 units
UPC / GTIN / UDI-DI10889942337033, 10889942405527, 10889942540570, 40889942337034, 40889942405528, 40889942540571
Lot numbers22IBH073, 22IBH620, 22JBU981, 22KBU236, 22LBB186, 23BBE163, 23BBQ244, 23BBT094, 23CBN156, 23DBO047, 23EBN965, 23FBG730, 23FBP998, 23HBL275, 23KBD992, 24BBT133, 24DBC913, 24DBM253, 24EBD055, 24EBM619, 24FBC811, 24GBO792, 24HBQ429, 24JBO656, 24KBI875, 24KBO162, 25ABG686, 25ABL984, 25ABV250, 25BBC496, 25BBG137, 25BBI161, 25BBS716, 25BBU979, 25CBB632, 25CBC880, 25CBN329, 25DBR721
Model numbersDYNJSYR10CWRB, VASC1018A, VASCSLPOFF1

Product

Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB; 2) MANIFOLD KIT LOW PRESSURE OFF, Model Number: VASCSLPOFF1; 3) EP MANIFOLD KIT, Model Number: VASC1018A

Reason for recall

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

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-1833-2026. 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.