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.
Reported: February 3, 2021 Initiated: September 4, 2020 #Z-0930-2021
Product Description
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.
Reason for Recall
Recalled products do not have FDA approval for sale in the United States.
Details
- Recalling Firm
- Braxton Medical Corporation
- Units Affected
- 1,781 cases
- Distribution
- 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.
- Location
- Lutz, FL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Braxton Medical Corporation. Units affected: 1,781 cases.
Why was this product recalled? ▼
Recalled products do not have FDA approval for sale in the United States.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 3, 2021. Severity: Moderate. Recall number: Z-0930-2021.
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