Alfa Wassermann Diagnostic Technologies recall
Alfa Wassermann Diagnostic Technologies, LLC. ACE ALT Reagent. Product Usage: For quantitative determination of ALT in serum and lithium heparin…
Why was Alfa Wassermann Diagnostic Technologies recalled?
Extremely low absorbance readings.
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?
ACE¿ ALT Reagent (Product reorder number SA1046 Lot F3604)
- Product
- Alfa Wassermann Diagnostic Technologies, LLC. ACE ALT Reagent. Product Usage: For quantitative determination of ALT in serum and lithium heparin…
- Recalling firm
- Alfa Wassermann, Inc.
- Quantity
- 731 Kits
- Distribution
- US Nationwide Distribution
- Recall date
- May 7, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)