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Braxton Medical Corporation recalls B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and
Recalled February 3, 2021 · FDA recall Z-0930-2021 · Braxton Medical
Hazard
Recalled products do not have FDA approval for sale in the United States. · FDA Class II
Units
1,781 cases
Sold at
US Nationwide distribution including in the states of AL, CA, CT, FL, GA, IL, KS, LA, MI, MN, NC, NJ, NY, PA, SD, TX, WA.
Description
Recalled products do not have FDA approval for sale in the United States.
Product
B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and tissue access to sample blood, monitor blood pressure, or administer fluids and blood intravascular.
Manufacturer(s)
Braxton Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →