Syeda (drospirenone and ethinyl estradiol) recall
Syeda (drospirenone and ethinyl estradiol), 3 mg/0.03 mg, 3 x 28 tablet blistercards, combination oral contraceptive tablet, Manufactured by…
Why was Syeda (drospirenone and ethinyl estradiol) recalled?
Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could contain the incorrect debossing on one side of the tablet U2 instead of U3.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
LF01215A, Exp 02/2014
- Product
- Syeda (drospirenone and ethinyl estradiol), 3 mg/0.03 mg, 3 x 28 tablet blistercards, combination oral contraceptive tablet, Manufactured by…
- Recalling firm
- Sandoz Incorporated
- Quantity
- 17,188 cartons containing 3 cards each.
- Distribution
- Nationwide
- Recall date
- February 13, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)