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Class II: temporary or reversible health riskOngoing

Preferred Pharmaceuticals Atorvastatin Calcium Tablets Recall

Atorvastatin Calcium Tablets, USP, 20 mg, packaged in: a) 90-count bottle (NDC 68788-76…

Preferred Pharmaceuticals, Inc. · Anaheim, CA

Risk level
Class II
Reported by FDA
Apr 12, 2023
Recall ID
D-0512-2023
Check your lot numberHow we source this data

Summary

Preferred Pharmaceuticals recalled Atorvastatin Calcium Tablets starting Mar 23, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0512-2023 on Apr 12, 2023. Reason: cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection. Status: Ongoing.

Why it was recalled

cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.

Product description

Atorvastatin Calcium Tablets, USP, 20 mg, packaged in: a) 90-count bottle (NDC 68788-7631-9); b) 30-count bottle (NDC 68788-7631-3), Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703

Lot numbers, UPCs & expiration codes

a) Lot: B1522B, Exp 4/30/2023; lot:C0222H, C0322B, Exp 5/31/2023; lot: E1022H, F13220, H2222P, Exp 6/30/2023; Lot: I1422V, K01220, Exp 12/31/2023; Lot: L2722H, Exp 3/31/2024; b) Lot:C0322B, Exp 5/31/2023; lot:H1122G, 12322Q, Exp 6/30/2023; lot: J1222U, Exp 12/31/2023.

Where it was sold

USA Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0512-2023
Classification
Class II
Status
Ongoing
Recall initiated
Mar 23, 2023
FDA report date
Apr 12, 2023
Quantity
a) 375 Bottles b) 323 Bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Preferred Pharmaceuticals, Inc.

Original FDA data

Every field from FDA enforcement report D-0512-2023, exactly as published.

Show all FDA fields
City
Anaheim
State
CA
Status
Ongoing
Country
United States
Event ID
91952
Address
1250 N Lakeview Ave Ste O
Code information
a) Lot: B1522B, Exp 4/30/2023; lot:C0222H, C0322B, Exp 5/31/2023; lot: E1022H, F13220, H2222P, Exp 6/30/2023; Lot: I1422V, K01220, Exp 12/31/2023; Lot: L2722H, Exp 3/31/2024; b) Lot:C0322B, Exp 5/31/2023; lot:H1122G, 12322Q, Exp 6/30/2023; lot: J1222U, Exp 12/31/2023.
Postal code
92807-1801
Report date
Apr 12, 2023
Product type
Drugs
Recall number
D-0512-2023
Classification
Class II
Recalling firm
Preferred Pharmaceuticals, Inc.
Product quantity
a) 375 Bottles b) 323 Bottles
Reason for recall
cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Atorvastatin Calcium Tablets, USP, 20 mg, packaged in: a) 90-count bottle (NDC 68788-7631-9); b) 30-count bottle (NDC 68788-7631-3), Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703
Distribution pattern
USA Nationwide
Recall initiation date
Mar 23, 2023
Initial firm notification
Letter
Center classification date
Apr 6, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0512-2023, published Apr 12, 2023. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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