Reported Apr 29, 2026 · Ongoing
Medline Syringes
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline Syringes
10 of 10 products
| Model / number | Product as published |
|---|---|
DYNJSYR12CWR | SYRINGE 12ML CONTROL W/ROTATOR |
DYNJSYR10CWR | SYRINGE 10ML CONTROL W/ROTATOR |
DYNJSYR12CP | SYR CONTROL PAD 12ML L/L |
DYNJBRT72R | TBG PRESS 72IN M/F ROT BRAID |
DYNJSYR10C | SYRINGE 10ML CONTROL MLL |
DYNJSYR8C | SYRINGE 8ML CONTROL MLL |
DYNJSYR12C | SYRINGE 12ML CONTROL MLL |
DYNJSYR10CRP | SYR CONTROL PAD 10ML L/L ROT |
DYNJSYR12CRP | SYR CONTROL PAD 12ML L/L ROT |
DYNJSYRC6CWR | CTRL SYRINGE 6ML RING ROT L/L |
- Lot codes and dates
26 of 26 products
Products covered by this recall # Barcodes Product as published 1 1088438967648640884389676487Lot Number: 25ABF227; 2) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case) 2 1088438967648640884389676487Lot Number: 25CBC537; 3) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case) 3 1088438967648640884389676487Lot Number: 25EBK855; 4) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case) 4 1088438967648640884389676487Lot Number: 25IDA120; 5) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case) 5 1088438967648640884389676487Lot Number: 25IDA552; 6) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case) 6 1088438967648640884389676487Lot Number: 25IDA648; 7) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case) 7 1088438967272340884389672724Lot Number: 25IDB507; 8) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case) 8 1088438967272340884389672724Lot Number: 25EBH091; 9) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case) 9 1088438967272340884389672724Lot Number: 25EBO178; 10) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case) 10 1088438967272340884389672724Lot Number: 25IDA686; 11) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case) 11 1088438967272340884389672724Lot Number: 25JDA207; 12) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case) 12 1088827723661540888277236616Lot Number: 25JDB599; 13) DYNJSYR12CP, UDI-DI: 10888277236615(each), 40888277236616(case) 13 1088827723661540888277236616Lot Number: 25GBD528; 14) DYNJSYR12CP, UDI-DI: 10888277236615(each), 40888277236616(case) 14 1088438985421140884389854212Lot Number: 25JDB601; 15) DYNJBRT72R, UDI-DI: 10884389854211(each), 40884389854212(case) 15 1088438967646240884389676463Lot Number: 25GBN402; 16) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case) 16 1088438967646240884389676463Lot Number: 25GBS345; 17) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case) 17 1088438967646240884389676463Lot Number: 25GBS857; 18) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case) 18 1088438967646240884389676463Lot Number: 25GBU045; 19) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case) 19 1088438967649340884389676494Lot Number: 25GBV139; 20) DYNJSYR8C, UDI-DI: 10884389676493(each), 40884389676494(case) 20 1088438967647940884389676470Lot Number: 25IDB505; 21) DYNJSYR12C, UDI-DI: 10884389676479(each), 40884389676470(case) - Amount recalled
- 38,230 units
This recall covers 39 products
The agency filed one notice per product. You are reading one of them; the other 38 are below.
26 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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