BD MAX DNA MMK Lab Use recall
BD MAX DNA MMK Lab Use, catalog no. 442828
Why was BD MAX DNA MMK Lab Use recalled?
The package insert incorrectly lists the volume of the primer and probe diluent to use for the reconstitution of the master mix tube. Adding the incorrect amount of diluent could have an effect on the assay.
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?
All since 08/20/2014
- Product
- BD MAX DNA MMK Lab Use, catalog no. 442828
- Recalling firm
- Becton Dickinson & Co.
- Quantity
- N/A
- Distribution
- Distributed to accounts in 8 states: CA, FL, NJ, NY, OR, PA, VA, and WI. International distribution to Argentina, Australia, Brazil, Canada, Chile, China, Colombia, Europe, Hong Kong, Japan, Singapore, Taiwan, and Thailand.
- Recall date
- May 9, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)