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Class III: unlikely to cause harmTerminated

Watson Laboratories Caziant Recall

Caziant (desogestrel and ethinyl estradiol) Tablets, USP, (Triphasic Regimen), 0

Watson Laboratories Inc · Corona, CA

Risk level
Class III
Reported by FDA
Dec 26, 2012
Recall ID
D-094-2013
Check your lot numberHow we source this data

Summary

Watson Laboratories recalled Caziant starting Dec 13, 2012. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-094-2013 on Dec 26, 2012. Reason: Impurities/Degradation Products: Out-of-specification results were obtained for a known impurities. Status: Terminated.

Why it was recalled

Impurities/Degradation Products: Out-of-specification results were obtained for a known impurities.

Product description

Caziant (desogestrel and ethinyl estradiol) Tablets, USP, (Triphasic Regimen), 0.1 mg/0.025 mg, 0.125 mg/0.025 mg, 0.15 mg/0.025 mg, 28-count tablets per dispenser (NDC 52544-959-28), packaged in 3-count Tablet Dispensers per carton (NDC 52544-959-31), Rx only Manufactured by: Watson Laboratories, Inc., Corona, CA 92880; Distributed by: Watson Pharma, Inc., Corona, CA 92880.

Lot numbers, UPCs & expiration codes

432127A Exp. 01/13, 478076A Exp. 05/13, 515539B Exp.09/13

Where it was sold

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-094-2013
Classification
Class III
Status
Terminated
Recall initiated
Dec 13, 2012
FDA report date
Dec 26, 2012
Quantity
63,627 cartons
Recall type
Voluntary: Firm initiated
Recalling firm
Watson Laboratories Inc

Original FDA data

Every field from FDA enforcement report D-094-2013, exactly as published.

Show all FDA fields
City
Corona
State
CA
Status
Terminated
Country
United States
Event ID
63906
Address
311 Bonnie Cir
Code information
432127A Exp. 01/13, 478076A Exp. 05/13, 515539B Exp.09/13
Postal code
92880-2882
Report date
Dec 26, 2012
Product type
Drugs
Recall number
D-094-2013
Classification
Class III
Recalling firm
Watson Laboratories Inc
Product quantity
63,627 cartons
Termination date
Dec 4, 2013
Reason for recall
Impurities/Degradation Products: Out-of-specification results were obtained for a known impurities.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Caziant (desogestrel and ethinyl estradiol) Tablets, USP, (Triphasic Regimen), 0.1 mg/0.025 mg, 0.125 mg/0.025 mg, 0.15 mg/0.025 mg, 28-count tablets per dispenser (NDC 52544-959-28), packaged in 3-count Tablet Dispensers per carton (NDC 52544-959-31), Rx only Manufactured by: Watson Laboratories, Inc., Corona, CA 92880; Distributed by: Watson Pharma, Inc., Corona, CA 92880.
Distribution pattern
Nationwide
Recall initiation date
Dec 13, 2012
Initial firm notification
Letter
Center classification date
Dec 18, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-094-2013, published Dec 26, 2012. View the source record (openFDA) · FDA enforcement reports

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

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