E-Z-HD recall: Subpotent
E-Z-HD (barium sulfate) For Suspension (98% w/w), 340 g bottle, Rx Only, Manufactured by E-Z-EM Canada Inc., a subsidiary of E-Z-EM, Inc., Lake…
Why was E-Z-HD recalled?
Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.
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?
Lot #'s: 64205, 64206, 64200, 64201, 64202, 64203, 64204, 64207, 64264, Exp 05/15; 64265, 64267, 64268, 64270, 64271, Exp 06/15
- Product
- E-Z-HD (barium sulfate) For Suspension (98% w/w), 340 g bottle, Rx Only, Manufactured by E-Z-EM Canada Inc., a subsidiary of E-Z-EM, Inc., Lake…
- Recalling firm
- Bracco Diagnostic Inc
- Quantity
- 216,792 bottles
- Distribution
- Nationwide and Puerto Rico
- Recall date
- August 20, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)