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Politics

Ldl cholesterol Medicine Is Being Recalled Nationwide—Over 140,000 Bottles Affected

Madisony
Last updated: October 24, 2025 9:38 pm
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Ldl cholesterol Medicine Is Being Recalled Nationwide—Over 140,000 Bottles Affected
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Key Factors

  • A minimum of 141,984 bottles of ldl cholesterol medicine are being recalled nationwide.

  • The prescription impacted is Atorvastatin Calcium tablets offered in 90-count, 500-count and 1000-count packages.

  • Contact your healthcare supplier or pharmacy for a possible refund or alternative.

The U.S. Meals and Drug Administration introduced a recall on prescription statin medicine offered nationwide. This is because of “failed dissolution specs.”

The medication impacted by this recall are Atorvastatin Calcium tablets. A minimum of 141,984 bottles of the product are affected. Under is the listing 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 Rely

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

Verify your medicine, and if it matches any of the above recall data, contact your healthcare supplier or pharmacy for a alternative or potential refund. This recall was simply categorized as a Class II, that means that the recalled tablets could result in minor, non permanent well being issues.

For questions on this recall, contact the FDA at 1-888-INFO-FDA (1-888-463-6332).

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