Reported Feb 25, 2026 · Ongoing
Medline Industries IV Administration and Extension Sets
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 Industries IV Administration and Extension Sets
23 of 23 products
| Model / number | Product as published |
|---|---|
DYNDTB0529 | DBD-IV ADMIN SET,60DRP,1NEEDLE-FREE VALV |
DYNDTB1029 | IV ADMIN SET, 10DRP, 1NF, 92 |
DYNDTB1516 | DBD-IVEXTSET2.4ML2 NEEDLE-FREEVLVE,35 |
DYNDTB1530 | DBD-IV ADMIN SET, 15DRP, 1 INJECT PORT |
DYNDTB1539 | DBD-IV ADMIN SET, 15DRP, ROLLER CLAMP, 6 |
DYNDTB1545 | DBD-IV ADMIN SET, 15DRP, 3 NF, 109 |
DYNDTB2045 | IV ADMIN SET, 20DRP, 3 NF, 109 |
DYNDTB0512 | DBD-IVADMINSET60DRP2NEEDLE-FREEVLVE96 |
DYNDTB0555 | DBD-IVADMINSET,60DRP3 NEEDLE-FREE VLVE11 |
DYNDTB1022 | IV ADMIN SET, 10DRP, NF,INJ, 96 |
DYNDTB1512 | DBD-IV ADMIN SET, 15DRP, 2NF, 96 |
DYNDTB1529 | DBD-IV ADMIN SET, 15DRP, 1NF, 92 |
DYNDTB1537 | DBD-IV ADMIN SET, 15DRP, ROLLER CLAMP, 9 |
DYNDTB1540 | DBD-IV ADMIN SET, 15DRP, SECOND, 40 |
DYNDTB2029 | IV ADMIN SET, 20DRP, 1NF, 92 |
DYNDTB5077 | DBD-IV EXT SET, 6.5, 1.1ML, M LUERLOCK |
DYNDTB1045 | IV ADMIN SET, 10DRP, 3 NF, 109 |
DYNDTB1545D | DBD-IVADMISET15DRP4NEEDLEFREE VLVESTPCK1 |
DYNDTB2524 | IV ADMIN SET15DRPFLWCTRL1NEEDLEFREE VA |
DYNDTB1012 | IV ADMIN SET, 10DRP, 2NF, 96 |
- Lot codes and dates
- 1) DYNDTB0529
- UDI-DI
10197344105663(each)20197344105660(case)
- Lot NumberAll Lot Numbers; 2) DYNDTB1029
- UDI-DI
10197344076956(each)20197344076953(case)
- Lot NumberAll Lot Numbers; 3) DYNDTB1516
- UDI-DI
10197344105687(each)20197344105684(case)
- Lot NumberAll Lot Numbers; 4) DYNDTB1530
- UDI-DI
10197344105694(each)20197344105691(case)
- Lot NumberAll Lot Numbers; 5) DYNDTB1539
- UDI-DI
10197344008254(each)20197344008251(case)
- Lot NumberAll Lot Numbers; 6) DYNDTB1545
- UDI-DI
10197344098644(each)20197344098641(case)
- Lot NumberAll Lot Numbers; 7) DYNDTB2045
- UDI-DI
10197344077007(each)20197344077004(case)
- Lot NumberAll Lot Numbers; 8) DYNDTB0512
- UDI-DI
10197344105656(each)20197344105653(case)
- Lot NumberAll Lot Numbers; 9) DYNDTB0555
- UDI-DI
10197344105670(each)20197344105677(case)
- Lot NumberAll Lot Numbers; 10) DYNDTB1022
- UDI-DI
10197344076949(each)20197344076946(case)
- Lot NumberAll Lot Numbers; 11) DYNDTB1512
- UDI-DI
10197344098613(each)20197344098610(case)
- Lot NumberAll Lot Numbers; 12) DYNDTB1529
- UDI-DI
10197344098620(each)20197344098627(case)
- Lot NumberAll Lot Numbers; 13) DYNDTB1537
- UDI-DI
10197344008247(each)20197344008244(case)
- Lot NumberAll Lot Numbers; 14) DYNDTB1540
- UDI-DI
10197344098637(each)20197344098634(case)
- Lot NumberAll Lot Numbers; 15) DYNDTB2029
- UDI-DI
10197344076994(each)20197344076991(case)
- Lot NumberAll Lot Numbers; 16) DYNDTB5077
- UDI-DI
10197344098651(each)20197344098658(case)
- Lot NumberAll Lot Numbers; 17) DYNDTB1045
- UDI-DI
10197344076963(each)20197344076960(case)
- Lot NumberAll Lot Numbers; 18) DYNDTB1545D
- UDI-DI
10197344105700(each)20197344105707(case)
- Lot NumberAll Lot Numbers; 19) DYNDTB2524
- UDI-DI
10197344105717(each)20197344105714(case)
- Lot NumberAll Lot Numbers; 20) DYNDTB1012
- UDI-DI
10197344076932(each)20197344076939(case)
- Lot NumberAll Lot Numbers; 21) DYNDTB2012
- UDI-DI
10197344076970(each)20197344076977(case)
- Lot NumberAll Lot Numbers; 22) DYNDTB2022
- UDI-DI
10197344076987(each)20197344076984(case)
- Lot NumberAll Lot Numbers; 23) DYNDTB5081
- UDI-DI
10197344098668(each)20197344098665(case)
- Lot NumberAll Lot Numbers
- Amount recalled
- 926,227 units
This recall covers 43 products
The agency filed one notice per product. You are reading one of them; the other 42 are below.
30 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may result in a delay in patient treatment, blood loss, infection, an air embolism, and/or underdosage of medication.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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