RecallRadar

FDA Drug recall D-0875-2018

Allergan Taytulla Softgel Capsules, 1 mg/20 mcg, 6x28 blister card Physicians's Sample - Not for Sale Distributed by: Allergan USA INC Irvi…

On 2018-06-20 the FDA classified a Class I recall of Allergan Taytulla Softgel Capsules, 1 mg/20 mcg, 6x28 blister card Physicians's Sample - Not for Sale Distributed by: Allergan USA INC Irvi… by Allergan, citing contraceptive Tablets Out of Sequence.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0875-2018
ClassificationClass I
Statusterminated
Initiated2018-05-24
Published2018-06-20
Last updated2026-09-13 11:52 UTC
CompanyAllergan
DistributionUS

Product

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

Reason

Contraceptive Tablets Out of Sequence.

Identifiers

upc300235862290
ndc0023-5862-28
ndc0023-5862-30
ndc0023-5862-29
ndc0023-5862-31
ndc3002358622
code_infoLot# 5620706, Exp. 05/19

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0875-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.