Reported Apr 29, 2026 · Ongoing

Medline Namic Guidewires

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 Namic Guidewires

30 of 30 products

Products covered by this recall
Model / numberProduct as published
DYNJGWIRE20LGUIDEWIRE 3MMJ 0.035X260CM LT
DYNJHWIRE105GWIRE HYDRO 0.035 180CM ANG S
DYNJHWIRE107GWIRE HYDRO 0.035 260CM ANG S
DYNJHWIRE115GWIRE HYDRO 0.035 260CM STR S
DYNJHWIRE108GWIRE HYDRO 0.035 150CM STR
DYNJHWIRE104GWIRE HYDRO 0.035 150CM ANG S
DYNJHWIRE113GWIRE HYDRO 0.035 180CM STR S
DYNJHWIRE103GWIRE HYDRO 0.035 260CM ANGLE
DYNJGWIRE01LGDWIRE .035INX150CM 3MMJ LT
DYNJGWIRE03LGDWIRE .035INX180CM 3MMJ LT
DYNJHWIRE112GWIRE HYDRO 0.035 150CM STR S
DYNJHWIRE109GWIRE HYDRO 0.035 180CM STR
DYNJHWIRE102GWIRE HYDRO 0.035 210CM ANGLE
DYNJHWIRE106GWIRE HYDRO 0.035 210CM ANG S
DYNJHWIRE110GWIRE HYDRO 0.035 210CM STR
DYNJHWIRE121GWIRE,HYDRO,0.038,180CM,ANG S
DYNJHWIRE122GWIRE HYDRO 0.038 210CM ANG S
DYNJHWIRE118GWIRE HYDRO 0.038 210CM ANGLE
DYNJHWIRE127GWIRE HYDRO 0.038 260CM STR
DYNJHWIRE130GWIRE,HYDRO,0.038,210CM,STR S
Lot codes and dates

96 of 96 products

Products covered by this recall
#BarcodesProduct as published
11019532718895540195327188956Lot Number: 34125030001; 2) DYNJGWIRE20L, UDI-DI: 10195327188955(each), 40195327188956(case)
21019532718895540195327188956Lot Number: 34125040001; 3) DYNJGWIRE20L, UDI-DI: 10195327188955(each), 40195327188956(case)
31019532718895540195327188956Lot Number: 25DBG562; 4) DYNJGWIRE20L, UDI-DI: 10195327188955(each), 40195327188956(case)
41019532730163740195327301638Lot Number: 25DBM956; 5) DYNJHWIRE105, UDI-DI: 10195327301637(each), 40195327301638(case)
51019532730163740195327301638Lot Number: 34124110001; 6) DYNJHWIRE105, UDI-DI: 10195327301637(each), 40195327301638(case)
61019532730163740195327301638Lot Number: 24LBR925; 7) DYNJHWIRE105, UDI-DI: 10195327301637(each), 40195327301638(case)
71019532730218440195327302185Lot Number: 25IDB410; 8) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case)
81019532730218440195327302185Lot Number: 34124110001; 9) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case)
91019532730218440195327302185Lot Number: 23IBI440; 10) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case)
101019532730218440195327302185Lot Number: 23KBI254; 11) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case)
111019532730218440195327302185Lot Number: 24ABQ057; 12) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case)
121019532730218440195327302185Lot Number: 24ABR513; 13) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case)
131019532730218440195327302185Lot Number: 24GBL513; 14) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case)
141019532730602140195327306022Lot Number: 25JDA853; 15) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case)
151019532730602140195327306022Lot Number: 34124110001; 16) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case)
161019532730602140195327306022Lot Number: 23BBI300; 17) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case)
171019532730602140195327306022Lot Number: 24DBT361; 18) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case)
181019532730219140195327302192Lot Number: 24LBN513; 19) DYNJHWIRE108, UDI-DI: 10195327302191(each), 40195327302192(case)
191019532730219140195327302192Lot Number: 34124110001; 20) DYNJHWIRE108, UDI-DI: 10195327302191(each), 40195327302192(case)
201019532730219140195327302192Lot Number: 24DBG409; 21) DYNJHWIRE108, UDI-DI: 10195327302191(each), 40195327302192(case)
Amount recalled
74,085 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, 4:16 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.