FoodNov 13, 2019
Wawona Frozen Foods Season s Choice recall — FDA F-0437-2020
FDA sampling found Hepatitis A in frozen raspberries.
Class IFDA: TerminatedWawona Frozen Foods Inc.
Latest records
Latest recalls — page 1136
The newest recall records with useful source details are listed here.
FoodNov 13, 2019
Dollar General Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar recall — FDA F-0136-2020
Possible undeclared milk allergen in product.
Class IIFDA: TerminatedDollar General Corporation
DrugNov 13, 2019
Basic Reset CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD, 1 fl. oz. recall — FDA D-0194-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Basic Reset BIOGENYX True Full Spectrum CBD Oil Cinnamon, 1 fl. oz. (30 mL) bottle, 750 mg recall — FDA D-0197-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 75 mg, a.) 30 count bottles recall — FDA D-0173-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 150 mg, a.) 24 count bottles recall — FDA D-0177-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
RANITIDINE HYDROCHLORIDE Dr. Reddy's Ranitidine Capsules, USP 300 mg, a.) 30 count bottles recall — FDA D-0180-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 150 mg, a.) 24 count bottles recall — FDA D-0170-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
First Royal Care Co. LLC, dba Red Mountain S-MIC/B12(C)/CARNITINE 25/50/50/1/50MG/ML MDV INJ recall — FDA D-0274-2020
Lack of Assurance of Sterility
Class IIFDA: TerminatedFirst Royal Care Co. LLC, dba Red Mountain Compounding…
DrugNov 13, 2019
First Royal Care Co. LLC, dba Red Mountain S-TRIMIX various strengths to include:a) S-TRIMIX recall — FDA D-0297-2020
Lack of Assurance of Sterility
Class IIFDA: TerminatedFirst Royal Care Co. LLC, dba Red Mountain Compounding…
DrugNov 13, 2019
Basic Reset BIOGENYX True Full Spectrum CBD Oil Wintergreen, 1 fl. oz. (30 mL) bottle, 750 recall — FDA D-0195-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Basic Reset Nuovi Firming Masque, Renew and Reset, 2 fl. oz. 59 mL bottle, Made in USA recall — FDA D-0190-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
RANITIDINE HYDROCHLORIDE Dr. Reddy's: Ranitidine Capsules 150 mg, Rx a.) 60 count bottles recall — FDA D-0168-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 150 mg, a.) 95 count bottles recall — FDA D-0176-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Basic Reset BIOGENYX True Full Spectrum CBD Oil Natural Flavor, 1 fl. oz. (30 mL) bottle recall — FDA D-0196-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 150 mg, 190 count bottles (2x95) Tray recall — FDA D-0169-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Basic Reset CBD Reset 750 True Full Spectrum Wintergreen, 750 mg CBD, 1 fl. oz. (30 mL) recall — FDA D-0191-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 150 mg, a.) 24 count bottles recall — FDA D-0172-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 75 mg, a.) 30- count bottles recall — FDA D-0183-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Lupin Pharmaceuticals Cephalexin for Oral Suspension USP, 250 mg/5mL, 200 mL bottle recall — FDA D-0304-2020
Presence of Foreign substance: identified as a dead ant.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugNov 13, 2019
Cefdinir for Oral Suspension USP, 125 mg/5mL recall — FDA D-0306-2020
Presence of Foreign substance: identified as a dead ant.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 150 mg, a.) 24 count bottles recall — FDA D-0184-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Cefdinir for Oral Suspension USP, 250 mg/5mL,100 mL bottle recall — FDA D-0305-2020
Presence of Foreign substance: identified as a dead ant.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugNov 13, 2019
Basic Reset CBD Reset 750 True Full Spectrum Natural Flavor 750 mg CBD 1 fl. oz. (30 mL) recall — FDA D-0193-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
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Recent recall archives
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