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Class II: temporary or reversible health riskTerminated

Apotex Paroxetine HCL Controlled-Release Tablets 25 Recall

Paroxetine HCL Controlled-Release Tablets 25 mg, 30-count bottle, Rx only, Manufactured…

Apotex Inc.

Risk level
Class II
Reported by FDA
Sep 10, 2014
Recall ID
D-1576-2014
Check your lot numberHow we source this data

Summary

Apotex recalled Paroxetine HCL Controlled-Release Tablets 25 starting Mar 24, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1576-2014 on Sep 10, 2014. Reason: Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and solvents. Status: Terminated.

Why it was recalled

Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and solvents.

Product description

Paroxetine HCL Controlled-Release Tablets 25 mg, 30-count bottle, Rx only, Manufactured by GlaxoSmithKline, RTP, NC 27709, Manufactured for Apotex Corp., Weston, FL 33328, NDC 60505-3674-3

Lot numbers, UPCs & expiration codes

Lot # 2A002, Exp. 01/15 Lot # 2A003, Exp. 01/15 Lot # 2C004, Exp. 03/15 Lot # 2C005, Exp. 03/15 Lot # 2E008, Exp. 05/15 Lot # 2F009, Exp. 06/15 Lot # 2F010, Exp. 06/15 Lot # 2H011, Exp. 08/15 Lot # 2H012, Exp. 08/15 Lot # 2H013, Exp. 0815

Where it was sold

Nationwide and Puerto Rico

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-1576-2014
Classification
Class II
Status
Terminated
Recall initiated
Mar 24, 2014
FDA report date
Sep 10, 2014
Recall type
Voluntary: Firm initiated
Recalling firm
Apotex Inc.

Original FDA data

Every field from FDA enforcement report D-1576-2014, exactly as published.

Show all FDA fields
City
Toronto
Status
Terminated
Country
Canada
Event ID
68967
Address
150 Signet Drive
Code information
Lot # 2A002, Exp. 01/15 Lot # 2A003, Exp. 01/15 Lot # 2C004, Exp. 03/15 Lot # 2C005, Exp. 03/15 Lot # 2E008, Exp. 05/15 Lot # 2F009, Exp. 06/15 Lot # 2F010, Exp. 06/15 Lot # 2H011, Exp. 08/15 Lot # 2H012, Exp. 08/15 Lot # 2H013, Exp. 0815
Report date
Sep 10, 2014
Product type
Drugs
Recall number
D-1576-2014
Classification
Class II
Recalling firm
Apotex Inc.
Termination date
Sep 23, 2014
Reason for recall
Chemical Contamination: Product were manufactured with active pharmaceutical ingredient (API) batches contaminated with residual materials and solvents.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Paroxetine HCL Controlled-Release Tablets 25 mg, 30-count bottle, Rx only, Manufactured by GlaxoSmithKline, RTP, NC 27709, Manufactured for Apotex Corp., Weston, FL 33328, NDC 60505-3674-3
Distribution pattern
Nationwide and Puerto Rico
Recall initiation date
Mar 24, 2014
Initial firm notification
Letter
Center classification date
Sep 3, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1576-2014, published Sep 10, 2014. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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