Medline Syringes: 1) SYRINGE 12ML CONTROL W/ROTATOR — Class II medical device recall Z-1831-2026
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-1831-2026 |
|---|---|
| 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 | 38,230 units |
| UPC / GTIN / UDI-DI | 10884389672723, 10884389676462, 10884389676479, 10884389676486, 10884389676493, 10884389854211, 10888277236585, 10888277236592, 10888277236615, 10889942885732, 40884389672724, 40884389676463, 40884389676470, 40884389676487, 40884389676494, 40884389854212, 40888277236586, 40888277236593, 40888277236616, 40889942885733 |
| Lot numbers | 25ABF227, 25CBC537, 25EBH091, 25EBK855, 25EBO178, 25GBD528, 25GBN402, 25GBS345, 25GBS857, 25GBU045, 25GBV139, 25IDA120, 25IDA552, 25IDA648, 25IDA686, 25IDB505, 25IDB506, 25IDB507, 25JDA207, 25JDA208, 25JDA594, 25JDB599, 25JDB600, 25JDB601, 25JDB602, 25JDB827 |
| Model numbers | DYNJBRT72R, DYNJSYR10C, DYNJSYR10CRP, DYNJSYR10CWR, DYNJSYR12C, DYNJSYR12CP, DYNJSYR12CRP, DYNJSYR12CWR, DYNJSYR8C, DYNJSYRC6CWR |
Product
Medline Syringes: 1) SYRINGE 12ML CONTROL W/ROTATOR, Model Number: DYNJSYR12CWR; 2) SYRINGE 10ML CONTROL W/ROTATOR, Model Number: DYNJSYR10CWR; 3) SYR CONTROL PAD 12ML L/L, Model Number: DYNJSYR12CP; 4) TBG PRESS 72IN M/F ROT BRAID, Model Number: DYNJBRT72R; 5) SYRINGE 10ML CONTROL MLL, Model Number: DYNJSYR10C; 6) SYRINGE 8ML CONTROL MLL, Model Number: DYNJSYR8C; 7) SYRINGE 12ML CONTROL MLL, Model Number: DYNJSYR12C; 8) SYR CONTROL PAD 10ML L/L ROT, Model Number: DYNJSYR10CRP; 9) SYR CONTROL PAD 12ML L/L ROT, Model Number: DYNJSYR12CRP; 10) CTRL SYRINGE 6ML RING ROT L/L, Model Number: DYNJSYRC6CWR
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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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-1831-2026. 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.