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

VernoNewsBy VernoNewsOctober 24, 2025No Comments2 Mins Read
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Ldl cholesterol Medicine Is Being Recalled Nationwide—Over 140,000 Bottles Affected
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Key Factors

  • No less than 141,984 bottles of ldl cholesterol medicine are being recalled nationwide.

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

  • 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).

Learn the unique article on EatingWell

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