Why it was recalled
Contraceptive Tablets Out of Sequence.
Product description
Allergan Taytulla Softgel Capsules, 1 mg/20 mcg, 6x28 blister card Physicians's Sample - Not for Sale Distributed by: Allergan USA INC Irvine, CA 92612 NDC 0023-5862-28 (Blister Card) NDC 0023-5862-29 (Blister Carton) NDC 0023-5862-31 (Outer carton) UPC 300235862290
Lot numbers, UPCs & expiration codes
Lot# 5620706, Exp. 05/19
Where it was sold
US 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-0875-2018
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- May 24, 2018
- FDA report date
- Jun 20, 2018
- Quantity
- 168,768 blister cards (4,725,504 softgel capsules)
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Allergan, PLC.
Original FDA data
Every field from FDA enforcement report D-0875-2018, exactly as published.
Show all FDA fields
- City
- Madison
- State
- NJ
- Status
- Terminated
- Country
- United States
- Event ID
- 80136
- Address
- 5 Giralda Farms
- Code information
- Lot# 5620706, Exp. 05/19
- Postal code
- 07940-1027
- Report date
- Jun 20, 2018
- Product type
- Drugs
- Recall number
- D-0875-2018
- Classification
- Class I
- Recalling firm
- Allergan, PLC.
- Product quantity
- 168,768 blister cards (4,725,504 softgel capsules)
- Termination date
- May 19, 2022
- Reason for recall
- Contraceptive Tablets Out of Sequence.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Allergan Taytulla Softgel Capsules, 1 mg/20 mcg, 6x28 blister card Physicians's Sample - Not for Sale Distributed by: Allergan USA INC Irvine, CA 92612 NDC 0023-5862-28 (Blister Card) NDC 0023-5862-29 (Blister Carton) NDC 0023-5862-31 (Outer carton) UPC 300235862290
- Distribution pattern
- US Nationwide
- Recall initiation date
- May 24, 2018
- Initial firm notification
- Letter
- Center classification date
- Jun 15, 2018