NAMIC Angiographic Syringe — Class I medical device recall Z-1718-2026
Ongoing recall by Medline Industries, LP, reported 2026-04-15, distributed nationwide. Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotatin
| Recall number | Z-1718-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-02-27 |
| Classified | 2026-04-07 |
| Reported by FDA | 2026-04-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, JP, KR, LK, NL, PK, SG, SK |
| Quantity | 1,752,096 kits |
| UPC / GTIN / UDI-DI | 10193489040166, 10193489040197, 10193489040210, 10193489040234, 10193489040319, 10193489040333, 10193489040340, 10193489040388, 10193489040449, 10193489040456, 10193489040470, 10193489040579, 10193489040593, 10193489040685, 10193489040715, 10193489040739, 10193489040746, 10193489040753, 10193489040869, 10193489040876, 10193489040944, 10193489040975, 10193489040999, 10193489041071, 10193489041149 and 475 more |
| Lot numbers | 000, 0000, 0000068535, 0000068943, 0000068944, 0000068945, 0000069181, 0000069185, 0000069219, 0000069220, 0000069224, 0000069232, 0000069248, 0000069249, 0000069254, 0000069255, 0000069256, 0000069258, 0000069259, 0000069264, 0000069265, 0000069273, 0000069274, 0000069275, 0000069279, 0000069285, 0000069287, 0000069288, 0000069298, 0000069299, 0000069313, 0000069315, 0000069325, 0000069338, 0000069346, 0000069348, 0000069351, 0000069352, 0000069354, 0000069359 and 460 more |
Product
NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline SKU 70087107; 6. SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline SKU 70088007; 7. SYRINGE,10ML,PP/FR,RA,-,PKG, Medline SKU 70095007; 8. SYRINGE,10ML,PP/FG,RA,-,PKG, Medline SKU 70095107; 9. SYRINGE,12ML,W/RES,PP/FR,RA,PG, Medline SKU 70097007; 10. SYRINGE,12ML,PP/FG,RA,W/RES,-,PKG, Medline SKU 70097107; 11. SYRINGE,12ML,PP/FG,RA,W/O,RES, Medline SKU 70098107; 12. SYRINGE,20ML,TR/FR,RA,OEM,PG, Medline SKU 80075027; 13. SYRINGE,10ML,ANGIO,W/RA,-,OEM, Medline SKU 80085007; 14. SYRINGE,12ML,TR/FR,RA,OEM, Medline SKU 80087007; 15. SYRINGE,10ML,PP/FR,RA,-,OEM,-,PG, Medline SKU 80095007; 16. SYRINGE,10ML,PP/FG,RA,OEM,PG, Medline SKU 80095107; 17. SYRINGE,12ML,PP/FG,RA,-,OEM,-,PG, Medline SKU 80097107
Reason for recall
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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-1718-2026. 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.