Accutest Drug Test Cup 5+3 Product Usage: The Accutest recall
Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid detection of multiple drugs in human…
Why was Accutest Drug Test Cup 5+3 Product Usage: The Accutest recalled?
Product was released to market without the adulteration strip included in the product.
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?
Part Number: DS84S625, Lot Number: 174886 (US distribution only)
- Product
- Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid detection of multiple drugs in human…
- Recalling firm
- Ameditech Inc
- Quantity
- 40 kit boxes (1000 units)
- Distribution
- US in the state of California
- Recall date
- October 31, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)