Key Factors
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No less than 141,984 bottles of ldl cholesterol medicine are being recalled nationwide.
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The prescription impacted is Atorvastatin Calcium tablets bought in 90-count, 500-count and 1000-count packages.
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Contact your healthcare supplier or pharmacy for a possible refund or substitute.
The U.S. Meals and Drug Administration introduced a recall on prescription statin medicine bought nationwide. This is because of “failed dissolution specs.”
The medicine impacted by this recall are Atorvastatin Calcium tablets. No less than 141,984 bottles of the product are affected. Beneath is the record of ldl cholesterol medicine being recalled, together with lot codes and expiration dates that may be discovered on the bottles or packaging:
|
Product Description |
Tablet Depend |
Lot Numbers |
Expiration Dates |
|
Atorvastatin Calcium Tablets USP, 10 mg |
90-count; 500-count 1000-count |
25141249; 24144938; 24144868; 24144867; 24144458; 24143994; 24142987; 24143316 |
Feb. 2027; Nov. 2026; Sept. 2026; July 2026 |
|
Atorvastatin Calcium Tablets USP, 40 mg, Rx Solely |
90-count; 500-count 1000-count |
25140933; 25140477; 24144254; 24144163; 24143995 |
Feb. 2027; Dec. 2026; Oct. 2026; Sept. 2026 |
|
Atorvastatin Calcium Tablets USP, 20 mg, Rx Solely |
90-count; 500-count 1000-count |
25140150; 25140173; 25140172; 24144720; 24144798; 24144692; 24143755; 24143913; 24143754; 24143047; 24142936 |
Dec. 2026, Nov. 2026; Oct. 2026; Aug. 2026; July 2026; June 2026 |
|
Atorvastatin Calcium Tablets USP, 80 mg, Rx Solely |
90-count, 500-count |
25140249; 25140247; 24144999; 24144942; 24144845; 24144713; 24144652; 24143898; 24143412; 24143582 |
Dec. 2026; Nov. 2026; Oct. 2026; Aug. 2026 |
Examine your medicine, and if it matches any of the above recall data, contact your healthcare supplier or pharmacy for a substitute or potential refund. This recall was simply categorised as a Class II, that means that the recalled tablets could result in minor, momentary well being issues.
For questions on this recall, contact the FDA at 1-888-INFO-FDA (1-888-463-6332).
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