Recall Z-1422-2013— Becton Dickinson & Co.
Class II · Terminated
Class II FDA medical device recall by Becton Dickinson & Co., initiated 2013-04-12, terminated 2013-09-28. FDA's recall record names no specific 510(k) clearance for this event. Product: BBL DrySlide PYR Kit, catalog number 231747 Product Usage: Presumptive diagnostic aid for group A streptococci and group D enterococci bacteria.. Reason: In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories..
- Recalling firm
- Becton Dickinson & Co.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-04-12
- Terminated
- 2013-09-28
- Firm location
- Sparks, MD, United States
Product description
BBL DrySlide PYR Kit, catalog number 231747 Product Usage: Presumptive diagnostic aid for group A streptococci and group D enterococci bacteria.
Reason for recall
In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.
Data sourced from openFDA. This site is unofficial and independent of the FDA.