NAMIC Angiographic Control Syringe — Class I medical device recall Z-1713-2026
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-1713-2026 |
|---|---|
| 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 | 192,690 units |
| UPC / GTIN / UDI-DI | 10193489065855, 10193489065893, 10193489065916, 10193489066753, 10193489066791, 10193489066814, 20193489065913, 20193489066811, 30193489065859, 30193489065897, 30193489066757, 30193489066795 |
| Lot numbers | 0000077029, 0000078186, 0000080553, 0000080919, 0000081537, 0000081539, 0000082969, 0000084274, 0000084335, 0000084509, 0000085041, 0000086756, 0000086823, 0000087347, 0000088044, 0000089554, 0000089563, 0000094514, 0000094842, 0000095687, 0000096918, 0000097388, 0000099870, 0000101535, 0000101882, 0000102372, 0000103862, 0000105095, 0000105155, 0000105613, 0000106954, 0000107328, 0000108237, 0000109442, 0000109479, 0000111244, 0000112810, 0000112966, 0000113792, 0000114317 and 138 more |
Product
NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80083007; 5. SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80084007; 6. MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline SKU 80084017.
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-1713-2026. 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.