BZO Strip Dip Card recall
BZO Strip Dip Card (300ng/ml)*, Item No. 100170
Why was BZO Strip Dip Card recalled?
Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity for up to two (2) of the nineteen (19) Benzodiazepine (BZO) compounds for which specificity information is provided in the product insert. The particular BZO compounds for which there may be reduced reactivity are Clonazepam and Chlordiazepoxide.
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?
141233 141669 141790 141820 141958 142082 142531 142532 142835 143020 143471 143553 152021 152432 152546 153094 153538 152104
- Product
- BZO Strip Dip Card (300ng/ml)*, Item No. 100170
- Recalling firm
- Ameditech Inc
- Quantity
- 31,472 kits
- Distribution
- Nationwide Distribution.
- Recall date
- December 30, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)