drugs MODERATE Updated 2017-03-15

Sandoz Inc recalls Pioglitazone and Glimepiride Tablets, USP, 30 mg/4 mg, 30 co

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Recalled Product

Pioglitazone and Glimepiride Tablets, USP, 30 mg/4 mg, 30 count bottles, Rx only, Manufactured by Lek Pharmaceuticals d.d., Verovskova Ulica 57, Ljubljana, - SI-1526, Slovenia --- NDC 0781-5635-31

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Hazard / Issue

Failed Dissolution Specifications

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot FY3669 with expiry 11/2017

✅ What Should You Do?

  1. 1Stop taking this medication and contact your doctor or pharmacist immediately.
  2. 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
  3. 3Check the lot number on your bottle or packaging against the recalled lots listed above.
  4. 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
View official government recall