Drug Recall List
Drug Recall List Drug
Recall Details
Last Updated: January 2022
Contact
Date
Drug Recall Class*
Lexette (halobetasol propionate) CGMP Deviation 05186260450
Clobazam 07778905804
Failed Stability Specifications
Clobetasol Propionate 05074230450 05074230401
Brinzolamide 00591212779 00591212712
CGMP Deviations Defective Container
If you have questions about this recall, Mayne Pharma Inc, 844 825 8500
January 2022
If you have questions about this recall, Ingenus Pharmaceuticals LLC, 877-530-1633.
January 2022
If you have questions about this recall, Ingenus Pharmaceuticals LLC, 1-407-354-5740
January 2022
If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
January 2022
Class II
Class II
Class II
Class II
* Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
8.4% Sodium Bicarbonate 05175450011
Metformin 70518292000
Norepinephrine Bitartrate 00703115303
Lack of Assurance of Sterility CGMP Deviations Lack of Assurance of Sterility
If you have questions about this recall, Exela Pharma Sciences LLC, 1888-451-4321 If you have questions about this recall, RemedyRepack Inc., 1866-845-3791 If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
January 2022
January 2022
January 2022
Class II
Class II
Class II
MethylPREDNISolone Acetate 01671409001
Lack of Assurance of Sterility
If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
January 2022
Class II
Carbamazepine
Failed Dissolution Specifications
If you have questions
January Class
01366826801
about this recall,
2022
II
Torrent Pharma Inc, 1-
888-280-2040.
Clobetasol Propionate
Microbial Contamination of Non-
If you have questions
January Class
05167212593
Sterile Products
about this recall, Taro
2022
I
Pharmaceuticals U.S.A.,
Inc.,1-800-544-1449 ext
6066.
* Drug Recall Class
Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death.
Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious
adverse health consequences is remote.
Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
Pregabalin 04733568788
Lidocaine Hydrochloride 06373999764
Lidocaine Hydrochloride 06373999764
Betamethasone Dipropionate 05256502329
Penicillin V Potassium 00093412573 00093412574
Fexofenadine Hydrochloride 00904697940
Failed Tablet/Capsule Specifications Superpotent Drug
If you have questions about this recall, SUN PHARMACEUTICAL INDUSTRIES INC, 1-800818-4555 If you have questions about this recall, Teligent Pharma, 1-856-697-1441
January 2022
January 2022
Class II
Class II
Superpotent Drug
If you have questions about this recall, Teligent Pharma, 1-856-697-1441
January 2022
Class I
Failed Stability Specifications
If you have questions about this recall, Teligent Pharma, 1-856-697-1441
January 2022
Class II
Subpotent
If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
December Class
2021
II
Failed Impurities/Degradation Specifications
If you have questions about this recall, The Harvard Drug Group, 1800-875-0123.
December Class
2021
II
* Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
Clindamycin and Benzoyl Peroxide Gel 00781726368
Lidocaine Hydrochloride 05256500950
Lidocaine Hydrochloride 06373999764 05256500950
Cefixime 70518274902
Diclofenac Sodium 68788770701
Superpotent Drug Superpotent Drug CGMP Deviations
Failed Impurities/Degradation Specifications Defective container
Hydrocodone Bitartrate and Acetaminophen 03172299701
Product Mix-up
If you have questions about this recall, TOLMAR, Inc., 1-970-2124500 If you have questions about this recall, Teligent Pharma, 1-856-697-1441
December 2021
December 2021
Class II
Class I
If you have questions about this recall, Teligent Pharma, 1-856-697-1441
December Class
2021
II
If you have questions about this recall, RemedyRepack Inc., 1866-845-3791 If you have questions about this recall, Preferred Pharmaceuticals, Inc., 1714-777-3729 If you have questions about this recall, Ascent Pharmaceuticals, Inc., 1-631-851-0550
December Class
2021
II
December Class
2021
II
December Class
2021
II
* Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
Cefixime 06787758450
Ascorbic Acid
Diclofenac Sodium 05266500205 05266502505
Flocinolone Acetonide 06516270486 06516270386
Cefixime 06787758450
Tadalafil 01671407501 01671407701
Failed impurities/degradation specifications Lack of Assurance of Sterility
Defective Container
Subpotent Drug
Failed Impurities/Degradation Specifications
Incorrect Product Formulation
If you have questions about this recall, Ascend Laboratories, LLC, 1-201-476-1977 If you have questions about this recall, ASP Cares, 1-210-615-7400
December 2021
December 2021
Class II
Class II
If you have questions about this recall, Teligent Pharma, 1-856-697-1441
December Class
2021
II
If you have questions about this recall, Amneal Pharmaceuticals., 1-833582-0812. If you have questions about this recall, Ascend Laboratories LLC, 1-201-476-1977
December 2021
November 2021
Class II
Class II
If you have questions about this recall, SUN PHARMACEUTICAL INDUSTRIES INC, 1-800818-4555
November 2021
Class II
* Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
Ezetimibe and Simvastatin 05140719305
Ezetimibe and Simvastatin 05140719290 05140719205
Methocarbamol 07133517952 07133517954 07133517957
Irbesartan and Hydrochlorothiazide 06818041306 06818041309 06818041406 06818041409
Irbesartan 06818041006 06818041009 06818041106 06818041109 06818041206 06818041209
Failed Excipient Specification
cGMP Deviations
Labeling: Label Error on Declared Strength
If you have questions about this recall, Dr. Reddy's Laboratories, Inc., 1-888-375-3784 If you have questions about this recall, Dr. Reddy's Laboratories, Inc., 1-888-375-3784 If you have questions about this recall, 1-877885-0882.
November Class
2021
II
November Class
2021
II
November Class
2021
I
CGMP Deviations
If you have questions about this recall, Lupin Pharmaceuticals Inc.1410-576-2000 ext 3
November Class
2021
II
CGMP Deviations
If you have questions about this recall, Lupin Pharmaceuticals Inc.1410-576-2000 ext 3
November Class
2021
II
* Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
Ezetimibe and Simvastatin 04359874290 04359874210 04359874430 04359874490 04359874530 04359874590 04359874505 04359874330 04359874390 04359874305
Failed Excipient Specifications
If you have questions about this recall, Dr. Reddy's Laboratories, Inc., 1-888-375-3784
November Class
2021
II
Rocuronium Bromide 66794022841
Imipramine Pamoate
Omeprazole Delayed-Release 07000002321
Labeling: Label Lacks Warning or Rx Legend
Out of specification result observed in a dissolution test
If you have questions about this recall, Piramal Critical Care, Inc. 1-800-414-1901 If you have questions about this recall, Lupin Pharmaceuticals Inc.1410-576-2000 ext 3
October 2021
October 2021
CGMP Deviations
If you have questions about this recall, Dr. Reddy's Laboratories, Inc., 1-888-375-3784
October 2021
Class II
Class II
Class II
* Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
AirDuo Digihaler 232/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) 05931013606
Subpotent drug
If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
October 2021
Class II
AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) 05931012906
Subpotent drug
If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
October 2021
Class II
AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) 05931011106
Subpotent drug
If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
October 2021
Class II
AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) 05931053008
Subpotent drug
If you have questions about this recall, Teva Pharmaceuticals USA, 1-800-545-8800
October 2021
Class II
AirDuo Digihaler 113/14
Subpotent drug
If you have questions
October Class
(fluticasone propionate 113 mcg
about this recall,
2021
II
and salmeterol 14 mcg)
Teva Pharmaceuticals
05931052008
USA,
1-800-545-8800
* Drug Recall Class
Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death.
Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious
adverse health consequences is remote.
Class 3 Recall: Using the drug is not likely to cause adverse health consequences.
NOTE: This is not a complete list of all recalls. Please see >Drugs>Drug Safety and Availability> Drug Recalls for additional information.
................
................
In order to avoid copyright disputes, this page is only a partial summary.
To fulfill the demand for quickly locating and searching documents.
It is intelligent file search solution for home and business.
Related searches
- science diet recall list 2019
- hills dog food recall list 2019
- blood pressure drug recall 2019
- fda drug recall list 2018
- blood pressure drug recall list
- drug recall list 2018
- drug recall list
- fda drug recall list
- blood pressure drug recall cancer
- fda drug recall list 2019
- fda drug recall losartan 2018
- fda drug recall list 2020