BBL DrySlide Oxidase Kit recall
BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.
Why was BBL DrySlide Oxidase Kit recalled?
In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Oxidase kit - lot 2222008 with expiration date 08/31/13
- Product
- BBL DrySlide Oxidase Kit, catalog number 231746 Product Usage: Presumptive diagnostic aid for gram-negative bacteria.
- Recalling firm
- Becton Dickinson & Co.
- Quantity
- 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.
- Recall date
- June 5, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)