Gildess 24 FE 1.5/30 recall: Subpotent
Gildess 24 FE 1.5/30 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, (a)…
Why was Gildess 24 FE 1.5/30 recalled?
Subpotent Drug; Ethinyl Estradiol
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?
Lot Numbers (a) 4082018, 4082019, 4359320, 4461688, 4501285, 4501286 (b) 4028921, 4258629, 4359321, 4461689, 4501287, 4581736
- Product
- Gildess 24 FE 1.5/30 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, (a)…
- Recalling firm
- Par Pharmaceutical, Inc.
- Quantity
- 44,127 tablets
- Distribution
- Nationwide and Puerto Rico
- Recall date
- November 9, 2016
- Classification
- Class III
- Status
- Completed
- Agency
- FDA (drug)