DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Beach Defense water+sun protection sunscreen spray recall — FDA D-0848-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
Monthly breakdown
2021 recalls by month
Select a month to review the recall records reported during that period.
December 2021194 records · 4 categoriesNovember 2021210 records · 4 categoriesOctober 2021342 records · 4 categoriesSeptember 2021300 records · 4 categoriesAugust 2021279 records · 4 categoriesJuly 2021251 records · 4 categoriesJune 2021361 records · 4 categoriesMay 2021226 records · 4 categoriesApril 2021279 records · 4 categoriesMarch 2021241 records · 4 categoriesFebruary 2021320 records · 4 categoriesJanuary 2021226 records · 4 categories
2021 recalls — page 31
Records are ordered by the best available source date.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 45 recall — FDA D-0837-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Aconitum Napellus Fear* 20% Alcohol HPUS: 5X, 6X, 26X, 30X recall — FDA D-0891-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
New Vision Pharmaceuticals Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 FL OZ recall — FDA D-0852-2021
Subpotent Drug
Class IIIFDA: TerminatedNew Vision Pharmaceuticals LLC
DrugOct 6, 2021
Washington Homeopathic Products Cedar Fever Drops, 20% USP ALCOHOL, 30 mL, homeopathic drug recall — FDA D-0862-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Viola Odorata 4X, 10X, 12X, Bee Stings*, Sucrose/Lactose recall — FDA D-0869-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Washington Homeopathic Products ZTE 1013 Formula Antimicrobial - F&M , Contents 1000 ml recall — FDA D-0887-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Aconitum nap Fear* 87% Alcohol HPUS: 5X, 7X, 18X, 30X recall — FDA D-0857-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 70 recall — FDA D-0838-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena COOLDRY SPORT sunscreen spray SPF 30, Avobenzone (3%) recall — FDA D-0832-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products ZTE-1035 Formula, Antimicrobial Combination, Contents 1006 recall — FDA D-0886-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Morphine Sulfate Injection, USP, 2 mg per mL, 1 mL single dose vial recall — FDA D-0856-2021
Defective container: Cracked vials leading to lack of sterility assurance
Class IIFDA: TerminatedFresenius Kabi USA LLC
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena COOLDRY SPORT WITH MICROMESH SUNSCREEN SPRAY Broad recall — FDA D-0842-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
New Vision Pharmaceuticals CVS Health Daytime Severe Cold & Flu Relief Single-Use Vials recall — FDA D-0853-2021
Subpotent Drug
Class IIIFDA: TerminatedNew Vision Pharmaceuticals LLC
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Beach Defense water+sun protection sunscreen spray recall — FDA D-0841-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Humulus 6X, 15X, Sucrose/Lactose Pills, 6X Packaged as a) recall — FDA D-0866-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Washington Homeopathic Products ZTE-1034 Formula Antimicrobial Bowel recall — FDA D-0885-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 50 recall — FDA D-0834-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products ZTE-105 Formula Gentle Detoxing recall — FDA D-0858-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 recall — FDA D-0836-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Beach Defense water+sun protection sunscreen spray recall — FDA D-0849-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Aconitum nap Fear* Sucrose/Lactose Pills HPUS: 4X, 5X recall — FDA D-0892-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Beach Defense water + sun protection sunscreen spray recall — FDA D-0833-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Johnson & Johnson Consumer Neutrogena Invisible Daily defense body spray sunscreen BROAD recall — FDA D-0843-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
About the 2021 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.