Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0 — Class II medical device recall Z-1829-2026
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-1829-2026 |
|---|---|
| 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 | 74,085 units |
| UPC / GTIN / UDI-DI | 10195327188955, 10195327301057, 10195327301590, 10195327301606, 10195327301613, 10195327301620, 10195327301637, 10195327302153, 10195327302184, 10195327302191, 10195327302207, 10195327302214, 10195327305987, 10195327305994, 10195327306007, 10195327306021, 10195327308308, 10195327308315, 10195327308414, 10195327308421, 10195327308438, 10195327308490, 10195327308506, 10195327308681, 10195327308698 and 33 more |
| Lot numbers | 23BBC807, 23BBE325, 23BBI300, 23BBI326, 23BBI328, 23EBB276, 23EBB277, 23EBB278, 23EBB282, 23EBB283, 23EBB284, 23EBB286, 23EBB287, 23EBB289, 23EBB291, 23EBB293, 23EBB296, 23EBB312, 23EBF993, 23EBF994, 23EBF995, 23EBG136, 23EBT183, 23EBW406, 23EBW407, 23EBW408, 23EBW411, 23EBW412, 23EBW413, 23EBW414, 23EBW417, 23EBW418, 23EBX142, 23EBX235, 23GBG005, 23GBO917, 23HBC832, 23HBG331, 23IBI440, 23JBI897 and 48 more |
| Model numbers | DYNJGWIRE01L, DYNJGWIRE03L, DYNJGWIRE20L, DYNJHWIRE100, DYNJHWIRE101, DYNJHWIRE102, DYNJHWIRE103, DYNJHWIRE104, DYNJHWIRE105, DYNJHWIRE106, DYNJHWIRE107, DYNJHWIRE108, DYNJHWIRE109, DYNJHWIRE110, DYNJHWIRE111, DYNJHWIRE112, DYNJHWIRE113, DYNJHWIRE115, DYNJHWIRE116, DYNJHWIRE118, DYNJHWIRE119, DYNJHWIRE120, DYNJHWIRE121, DYNJHWIRE122, DYNJHWIRE123 and 5 more |
Product
Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG S, Model Number: DYNJHWIRE105; 3) GWIRE HYDRO 0.035 260CM ANG S, Model Number: DYNJHWIRE107; 4) GWIRE HYDRO 0.035 260CM STR S, Model Number: DYNJHWIRE115; 5) GWIRE HYDRO 0.035 150CM STR, Model Number: DYNJHWIRE108; 6) GWIRE HYDRO 0.035 150CM ANG S, Model Number: DYNJHWIRE104; 7) GWIRE HYDRO 0.035 180CM STR S, Model Number: DYNJHWIRE113; 8) GWIRE HYDRO 0.035 260CM ANGLE, Model Number: DYNJHWIRE103; 9) GDWIRE .035INX150CM 3MMJ LT, Model Number: DYNJGWIRE01L; 10) GDWIRE .035INX180CM 3MMJ LT, Model Number: DYNJGWIRE03L; 11) GWIRE HYDRO 0.035 150CM STR S, Model Number: DYNJHWIRE112; 12) GWIRE HYDRO 0.035 180CM STR, Model Number: DYNJHWIRE109; 13) GWIRE HYDRO 0.035 210CM ANGLE, Model Number: DYNJHWIRE102; 14) GWIRE HYDRO 0.035 210CM ANG S, Model Number: DYNJHWIRE106; 15) GWIRE HYDRO 0.035 210CM STR, Model Number: DYNJHWIRE110; 16) GWIRE,HYDRO,0.038,180CM,ANG S, Model Number: DYNJHWIRE121; 17) GWIRE HYDRO 0.038 210CM ANG S, Model Number: DYNJHWIRE122; 18) GWIRE HYDRO 0.038 210CM ANGLE, Model Number: DYNJHWIRE118; 19) GWIRE HYDRO 0.038 260CM STR, Model Number: DYNJHWIRE127; 20) GWIRE,HYDRO,0.038,210CM,STR S, Model Number: DYNJHWIRE130; 21) GWIRE,HYDRO,0.038,260CM,ANG S, Model Number: DYNJHWIRE123; 22) GWIRE,HYDRO,0.038",150CM,STR, Model Number: DYNJHWIRE124; 23) GWIRE HYDRO 0.038 150CM ANGLE, Model Number: DYNJHWIRE116; 24) GWIRE,HYDRO,0.038",210CM,STR, Model Number: DYNJHWIRE126; 25) GWIRE HYDRO 0.035 260CM STR, Model Number: DYNJHWIRE111; 26) GWIRE HYDRO 0.035 150CM ANGLE, Model Number: DYNJHWIRE100; 27) GWIRE HYDRO 0.035 180CM ANGLE, Model Number: DYNJHWIRE101; 28) GWIRE,HYDRO,0.038",180CM, STR, Model Number: DYNJHWIRE125; 29) GWIRE HYDRO 0.038 260CM ANGLE, Model Number: DYNJHWIRE119; 30) GWIRE HYDRO 0.038 150CM ANG S, Model Number: DYNJHWIRE120
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-1829-2026. 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.