Why it was recalled
Cross Contamination With Other Products: The firm recalled Zovia, Lutera, Necon, and Zenchent, because certain lots could potentially be contaminated with trace amounts of Hydrochlorothiazide (HCTZ).
Product description
Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP, 1 mg/35 mcg, inert tablets, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA; Distributed by: Watson Pharma, Inc.; NDC 52544-383-28.
Lot numbers, UPCs & expiration codes
Lot #: 515622AA, 515623AA, and 515623BA, Exp 09/30/13
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-013-2013
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 19, 2012
- FDA report date
- Oct 31, 2012
- Quantity
- 30,267 cartons
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Watson Laboratories Inc
Original FDA data
Every field from FDA enforcement report D-013-2013, exactly as published.
Show all FDA fields
- City
- Corona
- State
- CA
- Status
- Terminated
- Country
- United States
- Event ID
- 63509
- Address
- 311 Bonnie Cir
- Code information
- Lot #: 515622AA, 515623AA, and 515623BA, Exp 09/30/13
- Postal code
- 92880-2882
- Report date
- Oct 31, 2012
- Product type
- Drugs
- Recall number
- D-013-2013
- Classification
- Class II
- Recalling firm
- Watson Laboratories Inc
- Product quantity
- 30,267 cartons
- Termination date
- Nov 21, 2013
- Reason for recall
- Cross Contamination With Other Products: The firm recalled Zovia, Lutera, Necon, and Zenchent, because certain lots could potentially be contaminated with trace amounts of Hydrochlorothiazide (HCTZ).
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP, 1 mg/35 mcg, inert tablets, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA; Distributed by: Watson Pharma, Inc.; NDC 52544-383-28.
- Distribution pattern
- Nationwide and Puerto Rico
- Recall initiation date
- Oct 19, 2012
- Initial firm notification
- Letter
- Center classification date
- Oct 24, 2012