DrugAug 21, 2019
Infusion Options METHOTREXATE 25 MG / 1 ML IM SYR recall — FDA D-1790-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
10,685drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 170
10,685 detailed records are currently available in this category.
DrugAug 21, 2019
Infusion Options DEXAMETHASONE 10 MG / 50 ML NS IVPB recall — FDA D-1767-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
US Pharmaceuticals Wonder Freeze Pain Releiving Gel with ILEX, Menthol 5% recall — FDA D-1740-2019
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 Cisplatin 40 MG / 500 ml NS IVPB WITH Mannitol 40 G recall — FDA D-1759-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
MAXIMUM STRENGTH HYDROCORTISONE CREAM WITH ALOE Hydrocortisone Cream With Aloe recall — FDA D-1731-2019
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
Tamsulosin Hydrochloride Capsules, USP 0.4 mg recall — FDA D-1844-2019
Failed Dissolution Specifications
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugAug 21, 2019
Clotrimazole and Betamethasone Dipropionate Cream USP, 1%/0.05%, 15 gram tubes recall — FDA D-1743-2019
Temperature Abuse: Complaints received of liquidy texture.
Class IIIFDA: TerminatedGlenmark Pharmaceuticals Inc., USA
DrugAug 21, 2019
Infusion Options Doxorubicin 110 MG / 55 ML IVP SYRINGE recall — FDA D-1770-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
Infusion Options PACLITAXEL ALBUMIN 185 mg /100 ml NS IVPB recall — FDA D-1799-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
US Pharmaceuticals CVS Health Glycerin Suppositories, 100- count box recall — FDA D-1736-2019
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 BORTEZOMIB 2.5 mg / 1 ML SQ SYRINGE recall — FDA D-1754-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
INTENSIVE HEALING ECZEMA Eczema Lotion Hydrocortisone 1% / Anti-Itch Lotion, 3.5 oz (99.2 g) recall — FDA D-1725-2019
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
MAXIMUM STRENGTH HYDROCORTISONE CREAM Hydrocortisone Cream, Hydrocortisone 1% / Anti-Itch recall — FDA D-1733-2019
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 RITUXAN 728 MG QS 728 mL 0.9% NACL IVPB recall — FDA D-1809-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
Infusion Options Doxorubicin Liposomal 71 MG / 250 ML D5W IVPB recall — FDA D-1771-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
DrugAug 21, 2019
MAXIMUM STRENGTH HYDROCORTISONE CREAM WITH ALOE Hydrocortisone Cream With Aloe recall — FDA D-1732-2019
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
US Pharmaceuticals Soothe&Cool Protect Moisture Guard Skin Protectant, 3.5 oz. (99 g), tube recall — FDA D-1735-2019
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
Lisinopril and Hydrochlorothiazide Tablets USP, 10 mg/12.5 mg, 100 tablet bottle recall — FDA D-1720-2019
Presence of Foreign Substance; Product complaints received related to brownish/blackish stains on the tablets and brownish/blackish powder observed inside the bottles.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugAug 21, 2019
Infusion Options NIVOLUMAB 480 MG / 100 ML NS IVPB recall — FDA D-1793-2019
Lack of Assurance of Sterility
Class IIFDA: TerminatedInfusion Options, Inc.
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.
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.
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.