Maalox recall: Labeling Error
Maalox, Regular Strength Antacid (calcium carbonate) chewable tablets, 600 mg, Wintergreen flavor, 50-count tablets per bottle, Novartis Consumer…
Why was Maalox recalled?
Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
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 #: 10095534, Exp 07/13; 10114311, Exp 04/14
- Product
- Maalox, Regular Strength Antacid (calcium carbonate) chewable tablets, 600 mg, Wintergreen flavor, 50-count tablets per bottle, Novartis Consumer…
- Recalling firm
- Novartis Consumer Health
- Quantity
- 46,680 bottles
- Distribution
- Nationwide, Canada, and Panama.
- Recall date
- August 28, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)