Recall Z-2325-2019— Becton Dickinson & Co.
Class II · Terminated
Class II FDA medical device recall by Becton Dickinson & Co., initiated 2019-07-17, terminated 2020-05-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Kit BD Max ExK DNA 2 USA; Catalog # 442819. Reason: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly..
- Recalling firm
- Becton Dickinson & Co.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-07-17
- Terminated
- 2020-05-13
- Firm location
- Sparks, MD, United States
Product description
Kit BD Max ExK DNA 2 USA; Catalog # 442819
Reason for recall
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Data sourced from openFDA. This site is unofficial and independent of the FDA.