Oxycodone Test Card recall
Oxycodone Test Card; LumiQuick,. Santa Clara, CA 95054
Why was Oxycodone Test Card recalled?
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
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?
Catalog number: 74044, All lots
- Product
- Oxycodone Test Card; LumiQuick,. Santa Clara, CA 95054
- Recalling firm
- LumiQuick Diagnostics Inc.
- Quantity
- ALL
- Distribution
- Distributed in the states of CA, FL, NJ, TX, and NY.
- Recall date
- April 16, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)