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

Products covered by this recall
Model / numberProduct as published
DYNJSYR12CWRSYRINGE 12ML CONTROL W/ROTATOR
DYNJSYR10CWRSYRINGE 10ML CONTROL W/ROTATOR
DYNJSYR12CPSYR CONTROL PAD 12ML L/L
DYNJBRT72RTBG PRESS 72IN M/F ROT BRAID
DYNJSYR10CSYRINGE 10ML CONTROL MLL
DYNJSYR8CSYRINGE 8ML CONTROL MLL
DYNJSYR12CSYRINGE 12ML CONTROL MLL
DYNJSYR10CRPSYR CONTROL PAD 10ML L/L ROT
DYNJSYR12CRPSYR CONTROL PAD 12ML L/L ROT
DYNJSYRC6CWRCTRL SYRINGE 6ML RING ROT L/L
Lot codes and dates

26 of 26 products

Products covered by this recall
#BarcodesProduct as published
11088438967648640884389676487Lot Number: 25ABF227; 2) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case)
21088438967648640884389676487Lot Number: 25CBC537; 3) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case)
31088438967648640884389676487Lot Number: 25EBK855; 4) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case)
41088438967648640884389676487Lot Number: 25IDA120; 5) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case)
51088438967648640884389676487Lot Number: 25IDA552; 6) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case)
61088438967648640884389676487Lot Number: 25IDA648; 7) DYNJSYR12CWR, UDI-DI: 10884389676486(each), 40884389676487(case)
71088438967272340884389672724Lot Number: 25IDB507; 8) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case)
81088438967272340884389672724Lot Number: 25EBH091; 9) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case)
91088438967272340884389672724Lot Number: 25EBO178; 10) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case)
101088438967272340884389672724Lot Number: 25IDA686; 11) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case)
111088438967272340884389672724Lot Number: 25JDA207; 12) DYNJSYR10CWR, UDI-DI: 10884389672723(each), 40884389672724(case)
121088827723661540888277236616Lot Number: 25JDB599; 13) DYNJSYR12CP, UDI-DI: 10888277236615(each), 40888277236616(case)
131088827723661540888277236616Lot Number: 25GBD528; 14) DYNJSYR12CP, UDI-DI: 10888277236615(each), 40888277236616(case)
141088438985421140884389854212Lot Number: 25JDB601; 15) DYNJBRT72R, UDI-DI: 10884389854211(each), 40884389854212(case)
151088438967646240884389676463Lot Number: 25GBN402; 16) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case)
161088438967646240884389676463Lot Number: 25GBS345; 17) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case)
171088438967646240884389676463Lot Number: 25GBS857; 18) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case)
181088438967646240884389676463Lot Number: 25GBU045; 19) DYNJSYR10C, UDI-DI: 10884389676462(each), 40884389676463(case)
191088438967649340884389676494Lot Number: 25GBV139; 20) DYNJSYR8C, UDI-DI: 10884389676493(each), 40884389676494(case)
201088438967647940884389676470Lot 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:59 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.