BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.
Reported: June 5, 2013 Initiated: April 12, 2013 #Z-1423-2013
Product Description
BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.
Reason for Recall
In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.
Details
- Recalling Firm
- Becton Dickinson & Co.
- Units Affected
- 610 total test kits (PYR and Oxidase)
- Distribution
- Worldwide Distribution - USA Nationwide and tthe countries of Australia, Canada, Europe, Hong Kong, Mexico, New Zealand, Singapore, and Taiwan.
- Location
- Sparks, MD
Frequently Asked Questions
What product was recalled? ▼
BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.. Recalled by Becton Dickinson & Co.. Units affected: 610 total test kits (PYR and Oxidase).
Why was this product recalled? ▼
In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 5, 2013. Severity: Moderate. Recall number: Z-1423-2013.
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