Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.
Reported: October 12, 2022 Initiated: September 1, 2022 #Z-0009-2023
Product Description
Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.
Reason for Recall
Potential for leakage at the catheter hub.
Details
- Recalling Firm
- B Braun Medical Inc
- Units Affected
- 94,000 US
- Distribution
- Domestic distribution to AZ CA FL GA MD MI MO MS NC NY OH PA TN TX WA. Foreign distribution to Canada
- Location
- Breinigsville, PA
Frequently Asked Questions
What product was recalled? ▼
Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.. Recalled by B Braun Medical Inc. Units affected: 94,000 US.
Why was this product recalled? ▼
Potential for leakage at the catheter hub.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 12, 2022. Severity: Moderate. Recall number: Z-0009-2023.
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