RecallRadar

FDA Drug recall D-0034-2027

Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro Pharmaceuticals Inc., B…

On 2026-10-14 the FDA classified a Class III recall of Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro Pharmaceuticals Inc., B… by Sun Pharmaceutical Industries, citing failed Impurities/Degradation Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0034-2027
ClassificationClass III
Statusongoing
Initiated2026-09-25
Published2026-10-14
Last updated2026-10-21 05:30 UTC
CompanySun Pharmaceutical Industries
DistributionUS

Product

Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Product of Canada, NDC 16714-249-02.

Reason

Failed Impurities/Degradation Specifications

Identifiers

ndc16714-249-01
ndc16714-249-02
code_infoLot # AD96183, Exp Date: 12/31/2026.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-21 05:30 UTC. Current status: ongoing.

Other recalls by Sun Pharmaceutical Industries

All Sun Pharmaceutical Industries recalls

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0034-2027%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.