Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)
Reported: July 27, 2022 Initiated: May 9, 2022 #Z-1440-2022
Product Description
Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)
Reason for Recall
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 40,050
- Distribution
- Worldwide distribution - US Nationwide distribution in the states of AK, AR, AZ, CA, CO, FL, GA, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NV, NY, OH, OR, PA, SD, TN, TX, UT, VA, WA, WV and the countries of Belgium, China, India, Indonesia, Japan, Korea, Nepal, Philippines, Singapore, Sri Lanka, Thailand, Vietnam.
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS). Recalled by Becton Dickinson & Company. Units affected: 40,050.
Why was this product recalled? ▼
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 27, 2022. Severity: Moderate. Recall number: Z-1440-2022.
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