Aurolife Pharma, LLC: 9 recalls on record

Recalls filed with 1 agency: FDA (9).

First recall on record: September 25, 2019. Most recent: June 28, 2023.

Risk classification: Class II: 8 · Class III: 1

Most recent recalls

DateAgencyProduct
June 28, 2023FDAGlycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo …D-0877-2023
December 28, 2022FDAGlycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma…D-0087-2023
April 6, 2022FDAGlycopyrrolate Tablets, USP, 1 mg, 100-count bottle, Rx Only, Distributed by: Aurobindo P…D-0736-2022
September 25, 2019FDAWal-Fex (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 5-count cartons, Distributed By…D-1873-2019
September 25, 2019FDAAllergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count cartons, DISCOUNT drug…D-1874-2019
September 25, 2019FDAFexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 6201…D-1870-2019
September 25, 2019FDAAllergy Relief (fexofenadine hydrochrloride) tablets, 180 mg, 5-count carton, Good Neighb…D-1866-2019
September 25, 2019FDAfexofenadine hydrochloride tablets USP, 180 mg, 150-count bottle, Member's Mark, Distribu…D-1867-2019
September 25, 2019FDAFexofenadine HCL Tablets USP, 180 mg, 500's BRITE STOCK; Manufactured for: Aurohealth LLC…D-1871-2019

Questions about this company

How many recalls does Aurolife Pharma, LLC have?
Recalert has 9 U.S. recalls on record for Aurolife Pharma, LLC, published between September 25, 2019 and June 28, 2023.
What was the most recent Aurolife Pharma, LLC recall?
FDA recall D-0877-2023, published June 28, 2023: Glycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01
Which agencies have handled Aurolife Pharma, LLC recalls?
Aurolife Pharma, LLC appears as the recalling firm in recalls from: FDA (9).

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