Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2021

Every FDA drug recall initiated in 2021, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,152 recalls, newest first.

Class II · Moderate risk

GaviLyteTM - C PEG-3350

Failed Stability Specification; Out of specification for Osmolarity

Terminated Stability / shelf life Novel Laboratories, Inc. d.b.a LUPIN NDC 43386-060-19 D-0726-2021
Class II · Moderate risk

Ethosuximide Oral Solution USP 250 mg/5 mL

Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.

Terminated cGMP deviation PAI Holdings, LLC. dba Pharmaceutical Associates Inc NDC 0121-0670-16 D-0723-2021
Class II · Moderate risk

Nystatin Oral Suspension

Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.

Terminated cGMP deviation PAI Holdings, LLC. dba Pharmaceutical Associates Inc NDC 0121-0868-16 D-0721-2021
Class II · Moderate risk

Venlafaxine Tablets

Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg

Terminated Labeling / mix-up Sun Pharmaceutical Industries INC NDC 16714-657-01 D-0703-2021
Class II · Moderate risk

GoodSense Aller.Ease

Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

Terminated Impurity / degradation Perrigo Company PLC NDC 0113-0571-30 D-0357-2022
Class II · Moderate risk

CVS Allergy Relief

Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

Terminated Impurity / degradation Perrigo Company PLC NDC 69842-698-39 D-0356-2022
Class II · Moderate risk

Kirkland Aller-Fex

Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

Terminated Impurity / degradation Perrigo Company PLC NDC 63981-571-48 D-0355-2022

Recalls by year