DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets 75 mg, a.) 30 count bottles (NDC 63868-482-30) recall — FDA D-0175-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
10,685drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 163
10,685 detailed records are currently available in this category.
DrugNov 13, 2019
Basic Reset Nuovi Skin Toner, Refined Ionyte, 4 FL recall — FDA D-0189-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Basic Reset Earth Wash Cleaner and Personal Care, Eco Friendly, Non Toxic, 2 fl.oz. bottle recall — FDA D-0187-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset 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.
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
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, 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
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
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
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
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, 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 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, 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
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
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
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
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
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
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
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-0177-2020
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-0173-2020
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 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.
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.