Lutz, FL, United States
Braxton Medical Corporation recalls
1 recall recorded since 2018, most recently on 4 September 2020. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 4 September 2020
- Reason
- Recalled products do not have FDA approval for sale in the United States.
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0930-2021
- 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.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.