Reported Mar 13, 2019 · Completed

Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged…

Apotex Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Apotex Inc. · 150 Signet Drive · North York, N/A · N/A

Is this the product you have?

  • Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged as 84 Tablets Blister, 3x1 Unit per carton (NDC 60505-4183-3), Rx Only
  • Manufactured forApotex Corp., Weston, FL 33326
  • Manufactured byOman Pharmaceutical Products Co. L.L.C., P.O. Box 1885, Postal Code 111, Seeb
Lot codes and dates
  • Lots
    • 7DY008A
    • 7DY009A
    • 7DY010A
    • 7DY011A
    • Exp. 08/2020
Amount recalled
82,705 cartons

Where it was sold

  • Nationwide

Why it was recalled

Contraceptive Tablets Out of Sequence: Missing or incorrect tablet placement.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Apotex Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 5:04 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.