Sandoz Inc Focalin XR 5 mg, 30 extended-release capsules per bottle recall: Labeling: Incorrect or Missing Lot and/or Exp Date
Labeling: Incorrect or Missing Lot and/or Exp Date
The hazard: Drug safety concern
The product was withdrawn from distribution. Whether your own pack is affected comes down to the lot number.
What the notice says: Labeling: Incorrect or Missing Lot and/or Exp Date
Why it matters: The FDA recorded an enforcement action against this product. The classification and the summary above describe how serious the agency considers it.
Recall details
- Recall number
- D-0608-2026
- Published
- June 24, 2026
- Risk level
- Class III
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Sandoz Inc
- Product type
- Prescription & OTC drugs
- Units affected
- 7,803 bottles
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot VA0099422; Exp. Date June 30, 2028
Products covered by this recall
Focalin XR (dexmethylphenidate HCl) 5 mg, 30 extended-release capsules per bottle, Rx only, Manufactured by Societal CDMO Gainesville, LLC, Gainesville, GA 30504. NDC: 66758-235-31
Check your product
The notice names 6 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Lot or batch code
Usually ink-stamped near the seam, the cap or the bottom of the pack.
- VA0099422
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- June 30
- 2028 — 7
- 803 bottles
NDC number
On the carton and again on the bottle or blister label.
- 66758-235-31
Package size
Match the net weight or the piece count on the front of the pack.
- 5 mg
Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Drug safety
Sandoz Inc — The product was withdrawn from distribution. Whether your own pack is affected comes down to the lot number.
- Check the lot number on your pack against the codes listed above.
- Keep the carton; the lot number is often printed only on the outer pack.
- Report side effects you think the product caused to FDA MedWatch.
- Do not stop a prescribed medicine on your own — speak to your prescriber or pharmacist first.
What the company owes you
A recalled medicine is the manufacturer’s cost to carry, not yours or your pharmacist’s.
- The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
- Ask the pharmacy to handle the claim where they can — they process recall returns in bulk and it saves you the correspondence.
- Keep the carton, the leaflet and the pharmacy label together until the claim is closed.
- Costs beyond the price of the medicine need to go to the company directly, in writing, with the recall number quoted.
Company contact: Sandoz Inc — 100 College Rd W, Princeton, NJ, 08540-6604
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Sandoz Inc prescription & otc drugs recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date Labeling: Incorrect or Missing Lot and/or Exp Date
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code VA0099422; best-by date June 30 or 2028 — 7. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Check the lot number on your pack against the codes listed above.
Can I get my money back?
The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
Where was the recalled product sold?
It was distributed nationwide.
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