Recall date: June 1, 2026Official recall - FDA Drug
Sandoz Focalin XR Capsules Recall
The FDA announced a recall of Focalin XR (dexmethylphenidate HCl) 5 Mg, 30 Extended-Release Capsules Per Bottle, Rx Only. The recall was issued because of labeling: Incorrect or Missing Lot and/or Exp Date. Please check the official recall notice for complete recommendations.
What matters now
- The recall involves Focalin XR (dexmethylphenidate HCl) 5 Mg, 30 Extended-Release Capsules Per Bottle, Rx Only.
- The recall was issued because of labeling: Incorrect or Missing Lot and/or Exp Date.
- June 1, 2026.
What product is included
The recall involves Focalin XR (dexmethylphenidate HCl) 5 Mg, 30 Extended-Release Capsules Per Bottle, Rx Only.
Why it was recalled
The recall was issued because of labeling: Incorrect or Missing Lot and/or Exp Date.
Action
If this may match your item
- Compare your item with the product name and affected-product details in the official notice.
- If your item matches, the official notice may include next steps such as using contact or reporting instructions. Please check the official recall notice for complete recommendations.
- If your item appears to match, keep the official source open while deciding what to do next.