DrugSmart 11 Test Cup recall
DrugSmart 11 Test Cup, Item No. 61127D; DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D; DrugSmart 9 Test Cup (BUP), Item No. 60960D; DrugSmart…
Why was DrugSmart 11 Test Cup recalled?
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
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?
140770 142294 151050 151527 142527 140998 142526 150596 151122 151196
- Product
- DrugSmart 11 Test Cup, Item No. 61127D; DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D; DrugSmart 9 Test Cup (BUP), Item No. 60960D; DrugSmart…
- Recalling firm
- Ameditech Inc
- Quantity
- 1220 units
- Distribution
- Worldwide Distribution - US (nationwide) and Internationally to Australia.
- Recall date
- November 25, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)