Medline Kits: 1) ANGIOGRAPHY PACK-LF — Class II medical device recall Z-1834-2026
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 number | Z-1834-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-02-25 |
| Classified | 2026-04-17 |
| Reported by FDA | 2026-04-29 |
| Distributed | Nationwide (US) |
| Quantity | 3,183 units |
| UPC / GTIN / UDI-DI | 10193489329698, 10193489449198, 10193489608816, 10193489651331, 10193489685923, 10193489774863, 10889942106691, 10889942145300, 10889942279777, 10889942592371, 10889942748426, 10889942846900, 40193489329699, 40193489449199, 40193489608817, 40193489651332, 40193489685924, 40193489774864, 40889942106692, 40889942145301, 40889942279778, 40889942592372, 40889942748427, 40889942846901 |
| Lot numbers | 21JBN533, 21KBM563, 21KBQ110, 21LBI454, 23DMF559, 23EMB053, 23FME913, 23GMC436, 23HME551, 23IBA898, 23JME012, 23KBL880, 24ABA125, 24BMK272, 24CMH245, 24CMK043, 24CMK043Z, 24DMJ156, 24FMI064, 24HMB643, 24JME212, 24KBE607, 25CBT538, 25DBQ486, 25DMB495, 25FBA222, 25FLA554, 25FMA232, 25GBF384, 25GBS720, 25ILA917, 25KBP615, 25LBQ639 |
| Model numbers | DYNJ31377B, DYNJ51279, DYNJ52447, DYNJ53369C, DYNJ53591A, DYNJ57516, DYNJ58722A, DYNJ62742, DYNJ67876, DYNJQ0505M, DYNJT2021G, VASC1170A |
Product
Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK, Model Number: DYNJT2021G; 3) ANGIOGRAPHY PACK, Model Number: DYNJ31377B; 4) ANGIO PACK, Model Number: DYNJ51279; 5) ANGIOGRAPHY PACK II, Model Number: DYNJ52447; 6) CATH ANGIO PACK, Model Number: DYNJ53369C; 7) ANGIO PACK, Model Number: DYNJ53591A; 8) ANGIOGRAPHIC PACK, Model Number: DYNJ57516; 9) ANGIOGRAPHY TRAY-LF, Model Number: DYNJ58722A; 10) ANGIO TRAY W/CHLORAPREP, Model Number: DYNJ62742; 11) CEREBRAL ANGIOGRAM, Model Number: DYNJ67876; 12) CSU CATH MANIFOLD KIT, Model Number: VASC1170A
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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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-1834-2026. 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.