Recall Z-1923-2013— Becton Dickinson & Company
Class II · Terminated
Class II FDA medical device recall by Becton Dickinson & Company, initiated 2013-05-01, terminated 2015-12-04. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes, NJ 07417 USA A sterile non-invasive device used to connect venous access devices such as needles, blood collection sets, ad infusion sets to blood collection tubes.. Reason: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood leakage and low draw volume..
- Recalling firm
- Becton Dickinson & Company
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-05-01
- Terminated
- 2015-12-04
- Firm location
- Franklin Lakes, NJ, United States
Product description
BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes, NJ 07417 USA A sterile non-invasive device used to connect venous access devices such as needles, blood collection sets, ad infusion sets to blood collection tubes.
Reason for recall
BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood leakage and low draw volume.
Data sourced from openFDA. This site is unofficial and independent of the FDA.