Mylan Pharmaceuticals Inc.: 79 recalls on record

Recalls filed with 1 agency: FDA (79).

First recall on record: October 3, 2012. Most recent: September 9, 2026.

Risk classification: Class I: 3 · Class II: 59 · Class III: 17

Most recent recalls

DateAgencyProduct
March 15, 2017FDAMirtazapine Tablets, USP 45 mg, a) 30 count, b) 100 count and c) 500 count bottles, Rx on…D-0492-2017
March 8, 2017FDAglipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceutic…D-0491-2017
November 30, 2016FDADiltiazem HCl Extended-release Capsules, USP 120 mg, 100-count bottle (NDC 0378-5220-01),…D-0151-2017
May 18, 2016FDAPaliperidone Extended-release Tablets, 1.5 mg, 30 count bottles, Rx only, Mylan Pharmaceu…D-0840-2016
July 15, 2015FDACapecitabine Tablets, USP, 500 mg, 120-count bottle, Rx only, Mylan Pharmaceuticals Inc.,…D-1217-2015
April 15, 2015FDAFexofenadine HCl Tablets, USP, 60 mg, Allergy, Antihistamine, Indoor and Outdoor Allergie…D-0435-2015
October 15, 2014FDAMetoprolol Succinate Extended-release Tablets, USP 50mg, 90-count Bottles, Rx only, Mfg …D-0009-2015
September 3, 2014FDADiltiazem HCl Extended Release Capsules, USP 120 mg, 500 count bottles, Rx only, Mylan Ph…D-1557-2014
August 27, 2014FDATolterodine Tartrate Tablets, 1 mg, 60 Tablet Bottles, Rx only. Mylan Pharmaceuticals In…D-1539-2014
February 19, 2014FDALevothyroxine Sodium Tablets, USP, 200 mcg, 100-count bottle, Rx only, Distributed by Myl…D-1084-2014
November 13, 2013FDAAmlodipine Besylate and Benazepril HCl Capsules, 10 mg/40 mg, 100-count bottles, Rx only,…D-66403-010
November 13, 2013FDALamotrigine Tablets, USP, 200 mg, packaged in a) 60-count bottles (NDC 0378-4254-91) and …D-66403-003
November 13, 2013FDAAmlodipine Besylate Tablets, USP, 2.5 mg, packaged in a) 90-count bottles (NDC 0378-5208-…D-66403-001
November 13, 2013FDAAmlodipine Besylate and Benazepril HCl Capsules, 5 mg/20 mg, packaged in a) 100-count bot…D-66403-007
November 13, 2013FDAAmlodipine Besylate Tablets, USP, 5 mg, packaged in a) 90-count bottles (NDC 0378-5209-77…D-66403-005
November 13, 2013FDAAmlodipine Besylate and Benazepril HCl Capsules, 5 mg/40 mg, 100-count bottles, Rx only, …D-66403-008
November 13, 2013FDAAmlodipine Besylate Tablets, USP 10 mg, packaged in a) 90-count bottles (NDC 0378-5210-77…D-66403-012
November 13, 2013FDACiprofloxacin Tablets, USP, 250 mg, 100-count bottles, Rx only, Mylan Pharmaceuticals Inc…D-66403-004
November 13, 2013FDAAmlodipine Besylate and Benazepril HCl Capsules, 10mg/20mg, in 100 count bottles (NDC# 03…D-66403-009
November 13, 2013FDAAmlodipine Besylate and Benazepril HCl Capsules, 5 mg/10 mg, packaged in a) 100-count bot…D-66403-006
November 13, 2013FDACiprofloxacin Tablets, USP, 500 mg,100-count bottles, Rx only, Mylan Pharmaceuticals Inc.…D-66403-011
November 13, 2013FDAAmlodipine Besylate and Benazepril HCl Capsules, 2.5 mg/10 mg, 100-count bottles, Rx only…D-66403-002
June 5, 2013FDARopinirole hydrochloride tablets, USP 4 mg, 100-count bottle (NDC 0378-5504-01), Rx only,…D-500-2013
May 1, 2013FDALisinopril Tablets, USP 10 mg, Rx only, 1000 count bottles, Manufactured for: Mylan Phar…D-269-2013
February 13, 2013FDALansoprazole Delayed-release Capsules, USP, 30 mg, 500-count capsules per bottle, Rx only…D-147-2013

Questions about this company

How many recalls does Mylan Pharmaceuticals Inc. have?
Recalert has 79 U.S. recalls on record for Mylan Pharmaceuticals Inc., published between October 3, 2012 and September 9, 2026.
Which agencies have handled Mylan Pharmaceuticals Inc. recalls?
Mylan Pharmaceuticals Inc. appears as the recalling firm in recalls from: FDA (79).

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