Breckenridge Pharmaceutical, Inc: 33 recalls on record

Recalls filed with 1 agency: FDA (33).

First recall on record: November 18, 2015. Most recent: June 17, 2026.

Risk classification: Class II: 31 · Class III: 2

Most recent recalls

DateAgencyProduct
March 22, 2023FDAAlprazolam Tablets, USP, 0.25mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0704-01…D-0458-2023
March 22, 2023FDAAlprazolam Tablets, USP, 1 mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0706-01),…D-0460-2023
March 22, 2023FDAAlprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01)…D-0459-2023
March 22, 2023FDAClobazam Tablets, 20 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmace…D-0463-2023
March 25, 2020FDASolifenacin Succinate Tablets, 5mg, packaged in a) 30-count bottles (NDC 51991-893-33) an…D-1050-2020
March 25, 2020FDASolifenacin Succinate Tablets, 10 mg, packaged in a) 30-count bottles (NDC 51991-894-33) …D-1051-2020
March 4, 2020FDAZoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL), Solution for Intravenous Infusion, St…D-1063-2020
November 18, 2015FDADuloxetine Delayed-release Capsules, USP, 60 mg, Rx Only, 1000 count bottle, Manufactured…D-0181-2016

Questions about this company

How many recalls does Breckenridge Pharmaceutical, Inc have?
Recalert has 33 U.S. recalls on record for Breckenridge Pharmaceutical, Inc, published between November 18, 2015 and June 17, 2026.
Which agencies have handled Breckenridge Pharmaceutical, Inc recalls?
Breckenridge Pharmaceutical, Inc appears as the recalling firm in recalls from: FDA (33).

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