DrugAug 21, 2019
Infusion Options RITUXIMAB 575 MG / 250 ml 0.9% NACL IVPB recall — FDA D-1810-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
10,690drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 171
10,690 detailed records are currently available in this category.
DrugAug 21, 2019
American Health Packaging Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg recall — FDA D-1820-2019
Failed Impurities/Degradation Specifications; out of specification result for an unknown impurity in stability samples.
Class IIFDA: TerminatedAmerican Health Packaging
DrugAug 21, 2019
MAXIMUM STRENGTH HYDROCORTISONE CREAM Hydrocortisone Cream, Hydrocortisone 1% / Anti-Itch recall — FDA D-1734-2019
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugAug 21, 2019
Infusion Options CARBOPLATIN 174 MG / 250ml NS IVPB recall — FDA D-1756-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
US Pharmaceuticals CVS Therapeutic Menthol Gel, 8 FL OZ (227 g) recall — FDA D-1726-2019
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugAug 21, 2019
WALGREENS ADULT GLYCERIN Adult Glycerin Suppositories, Package Size 25-count suppositories recall — FDA D-1728-2019
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugAug 21, 2019
Infusion Options Fluorouracil 560 MG / 11.2 ML IVP recall — FDA D-1777-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
Infusion Options ERIBULIN 1.12 MG / 100 ML NS IVPB recall — FDA D-1775-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
US Pharmaceuticals CVS Health Glycerin Suppositories, 50-count box recall — FDA D-1724-2019
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugAug 21, 2019
Infusion Options OXALIPLATIN 145 MG /250 ML D5W IVPB recall — FDA D-1797-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
US Pharmaceuticals Children Glycerin Suppositories Laxative for ages 2 to 5 recall — FDA D-1727-2019
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugAug 14, 2019
Herbal Doctor Remedies Worm Off, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies recall — FDA D-1620-2019
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugAug 14, 2019
AAA Pharmaceutical Smart Sense Regular Strength Aspirin Tablets, 325 mg packed in a) 100 recall — FDA D-1585-2019
Labeling; Incorrect or Missing Lot Number and/or Exp Date; Product has an incorrect expiration date of 9/2022 applied to the labeling, where the actual expiration date is 10/2021.
Class IIIFDA: TerminatedAAA Pharmaceutical, Inc.
DrugAug 14, 2019
Unipharma, LLC DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL recall — FDA D-1632-2019
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Class IIFDA: TerminatedUnipharma, LLC.
DrugAug 14, 2019
Unipharma, LLC CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl recall — FDA D-1631-2019
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Class IIFDA: TerminatedUnipharma, LLC.
DrugAug 14, 2019
Herbal Doctor Remedies Hair Back, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies recall — FDA D-1599-2019
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugAug 14, 2019
Lovastatin Tablets USP, 40 mg recall — FDA D-1584-2019
CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
Class IIIFDA: TerminatedAmerican Health Packaging
DrugAug 14, 2019
Herbal Doctor Remedies Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor recall — FDA D-1592-2019
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugAug 14, 2019
Unipharma, LLC CVS Health Children's Nasal Saline Drops with Himalayan Salt Saline Nasal recall — FDA D-1633-2019
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Class IIFDA: TerminatedUnipharma, LLC.
DrugAug 14, 2019
RXQ Compounding STERILE WATER FOR INJECTION USP, [10, 30, or 50 ML] per Vial, RXQ recall — FDA D-1707-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedRXQ Compounding LLC
DrugAug 14, 2019
Mometasone Furoate Cream USP, 0.1% recall — FDA D-1586-2019
GMP Deviations: Glenmark received complaints stating that mometasone fuorate cream was gritty.
Class IIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
DrugAug 14, 2019
Herbal Doctor Remedies Pain Away, 500 mg Capsules, 90-count bottles recall — FDA D-1611-2019
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugAug 14, 2019
Herbal Doctor Remedies Awake, 500 mg Capsules, 90-count bottles recall — FDA D-1589-2019
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Class IIFDA: TerminatedHerbal Doctor Remedies
DrugAug 14, 2019
Herbal Doctor Remedies Pain Stopper, 500 mg Capsules, 90-count bottles recall — FDA D-1612-2019
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Class IIFDA: TerminatedHerbal Doctor Remedies
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.