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
| Model / number | Product as published |
|---|---|
DYNJGWIRE20L | GUIDEWIRE 3MMJ 0.035X260CM LT |
DYNJHWIRE105 | GWIRE HYDRO 0.035 180CM ANG S |
DYNJHWIRE107 | GWIRE HYDRO 0.035 260CM ANG S |
DYNJHWIRE115 | GWIRE HYDRO 0.035 260CM STR S |
DYNJHWIRE108 | GWIRE HYDRO 0.035 150CM STR |
DYNJHWIRE104 | GWIRE HYDRO 0.035 150CM ANG S |
DYNJHWIRE113 | GWIRE HYDRO 0.035 180CM STR S |
DYNJHWIRE103 | GWIRE HYDRO 0.035 260CM ANGLE |
DYNJGWIRE01L | GDWIRE .035INX150CM 3MMJ LT |
DYNJGWIRE03L | GDWIRE .035INX180CM 3MMJ LT |
DYNJHWIRE112 | GWIRE HYDRO 0.035 150CM STR S |
DYNJHWIRE109 | GWIRE HYDRO 0.035 180CM STR |
DYNJHWIRE102 | GWIRE HYDRO 0.035 210CM ANGLE |
DYNJHWIRE106 | GWIRE HYDRO 0.035 210CM ANG S |
DYNJHWIRE110 | GWIRE HYDRO 0.035 210CM STR |
DYNJHWIRE121 | GWIRE,HYDRO,0.038,180CM,ANG S |
DYNJHWIRE122 | GWIRE HYDRO 0.038 210CM ANG S |
DYNJHWIRE118 | GWIRE HYDRO 0.038 210CM ANGLE |
DYNJHWIRE127 | GWIRE HYDRO 0.038 260CM STR |
DYNJHWIRE130 | GWIRE,HYDRO,0.038,210CM,STR S |
- Lot codes and dates
96 of 96 products
Products covered by this recall # Barcodes Product as published 1 1019532718895540195327188956Lot Number: 34125030001; 2) DYNJGWIRE20L, UDI-DI: 10195327188955(each), 40195327188956(case) 2 1019532718895540195327188956Lot Number: 34125040001; 3) DYNJGWIRE20L, UDI-DI: 10195327188955(each), 40195327188956(case) 3 1019532718895540195327188956Lot Number: 25DBG562; 4) DYNJGWIRE20L, UDI-DI: 10195327188955(each), 40195327188956(case) 4 1019532730163740195327301638Lot Number: 25DBM956; 5) DYNJHWIRE105, UDI-DI: 10195327301637(each), 40195327301638(case) 5 1019532730163740195327301638Lot Number: 34124110001; 6) DYNJHWIRE105, UDI-DI: 10195327301637(each), 40195327301638(case) 6 1019532730163740195327301638Lot Number: 24LBR925; 7) DYNJHWIRE105, UDI-DI: 10195327301637(each), 40195327301638(case) 7 1019532730218440195327302185Lot Number: 25IDB410; 8) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case) 8 1019532730218440195327302185Lot Number: 34124110001; 9) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case) 9 1019532730218440195327302185Lot Number: 23IBI440; 10) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case) 10 1019532730218440195327302185Lot Number: 23KBI254; 11) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case) 11 1019532730218440195327302185Lot Number: 24ABQ057; 12) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case) 12 1019532730218440195327302185Lot Number: 24ABR513; 13) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case) 13 1019532730218440195327302185Lot Number: 24GBL513; 14) DYNJHWIRE107, UDI-DI: 10195327302184(each), 40195327302185(case) 14 1019532730602140195327306022Lot Number: 25JDA853; 15) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case) 15 1019532730602140195327306022Lot Number: 34124110001; 16) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case) 16 1019532730602140195327306022Lot Number: 23BBI300; 17) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case) 17 1019532730602140195327306022Lot Number: 24DBT361; 18) DYNJHWIRE115, UDI-DI: 10195327306021(each), 40195327306022(case) 18 1019532730219140195327302192Lot Number: 24LBN513; 19) DYNJHWIRE108, UDI-DI: 10195327302191(each), 40195327302192(case) 19 1019532730219140195327302192Lot Number: 34124110001; 20) DYNJHWIRE108, UDI-DI: 10195327302191(each), 40195327302192(case) 20 1019532730219140195327302192Lot 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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