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.
10,685drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 112
10,685 detailed records are currently available in this category.
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 COOLDRY SPORT WITH MICROMESH SUNSCREEN SPRAY Broad recall — FDA D-0842-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, 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
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
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
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
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
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 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 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
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 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
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
Johnson & Johnson Consumer Neutrogena Beach Defense water+sun protection sunscreen spray recall — FDA D-0848-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Yeast Guard Blend, Calcarea Carbonica 6X, Collinsonia recall — FDA D-0860-2021
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-0846-2021
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-0844-2021
Chemical Contamination: presence of benzene
Class IFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products Strophanthus hisp 30X, Hives*, 20% Alcohol recall — FDA D-0889-2021
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 Z-1050 Formula Hepatodetox recall — FDA D-0883-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
SigmaPharm Laboratories Sodium Phenylbutyrate Powder, 250 Grams recall — FDA D-0898-2021
Failed Impurities/Degradation Specifications; Out of Specification impurity results obtained during routine testing.
Class IIFDA: TerminatedSigmaPharm Laboratories LLC
DrugOct 6, 2021
Johnson & Johnson Consumer Aveeno Protect + Refresh sunscreen weightless spray with oat SPF recall — FDA D-0831-2021
cGMP Deviations
Class IIFDA: OngoingJohnson & Johnson Consumer, Inc.
DrugOct 6, 2021
Washington Homeopathic Products ZTE-1020 Formula. Contents 1000ml. WHP Homeopathic Medicine recall — FDA D-0881-2021
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class IIFDA: TerminatedWashington Homeopathic Products, Inc.
DrugOct 6, 2021
American Health Packaging Valproic Acid Oral Solution, USP, 500 mg/10 mL, 100 10 mL unit recall — FDA D-0854-2021
CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Class IIFDA: TerminatedAmerican Health Packaging
How to use this drug recall index
A drug recall record can include the reason for recall, firm, status, distribution pattern, quantity and FDA classification. This site does not provide medical advice; it organizes public recall information and links users back to official sources.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
What the database can and cannot tell you
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.