FDADecember 4, 2019device
0.035"(.89mm)x80 cm guidewire. Model 114135080. Soft Tip 3.5cm. REF/UDI: 114135080/(01)208863333008067. RxOnly STERILE EO
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The stiffness of the soft end of the guidewire caused tissue perforation.
What to do
FDA enforcement status: Terminated
Brands named
argon medical devicesargonargon medical
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDALidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S. Korea, NDC 65282-1605-1.2026-05-12
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