DrugJul 29, 2015
Wockhardt Usa Zonisamide Capsules, 25 mg Capsules recall — FDA D-1274-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
10,690drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 296
10,690 detailed records are currently available in this category.
DrugJul 29, 2015
Wockhardt Usa Amlodipine Besylate Tablets, 5 mg Tablets, Packaged as A) 90 Count Bottles recall — FDA D-1255-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
DrugJul 29, 2015
Wockhardt Usa Zonisamide Capsules, 100 mg Capsules recall — FDA D-1254-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
DrugJul 29, 2015
Wockhardt Usa Captopril Tablets, USP, 50 mg Tablets recall — FDA D-1276-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
DrugJul 29, 2015
Wockhardt Usa Metoprolol Succinate Extended-Release Tablets, USP, 100 mg Tablets recall — FDA D-1270-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
DrugJul 29, 2015
Wockhardt Usa Lisinopril Tablets USP, 30 mg Tablets recall — FDA D-1260-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
DrugJul 29, 2015
Wockhardt Usa Famotodine Tablets, USP, 10 mg Tablets, For Repacking Only recall — FDA D-1267-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
DrugJul 29, 2015
Wockhardt Usa Lisinopril Tablets USP, 10 mg Tablets recall — FDA D-1258-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedWockhardt Usa Inc.
DrugJul 22, 2015
American Health Packaging Desmopressin Acetate Tablets, 0.1 mg Tablets recall — FDA D-1235-2015
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Class IIIFDA: TerminatedAmerican Health Packaging
DrugJul 22, 2015
Kremers Urban Pharmaceuticals Nitroglycerin Transdermal System 0.4 mg/hr (18 cm2), For recall — FDA D-1237-2015
Failed Impurities/Degradation Specifications: Two lots failed specification for unknown impurity at the 24 month stability testing.
Class IIFDA: TerminatedKremers Urban Pharmaceuticals, Inc.
DrugJul 22, 2015
Rifampin for Injection, USP 600mg/vial in a 20mL vial recall — FDA D-1234-2015
Failed Impurities/Degradation Specifications; out-of-specification for color, impurity, and degradation
Class IIFDA: TerminatedFresenius Kabi USA, LLC
DrugJul 22, 2015
KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M recall — FDA D-1241-2015
Crystallization; identified as calcium salt of Ketorolac
Class IIFDA: OngoingHospira Inc.
DrugJul 22, 2015
Geritrex Carb-O-Philic 40 Cream, 40%, a) 3 oz. tube (NDC 54162-640-03) b) 7 oz. tube recall — FDA D-1238-2015
CGMP Deviation: Poor container closure of the bulk storage container
Class IIIFDA: TerminatedGeritrex Corp
DrugJul 22, 2015
KETOROLAC Tromethamine Inj., USP, 60 mg (30 mg/mL), 2 mL Fill Single-dose Vials, I.V/I.M recall — FDA D-1242-2015
Crystallization; identified as calcium salt of Ketorolac
Class IIFDA: OngoingHospira Inc.
DrugJul 22, 2015
Kremers Urban Pharmaceuticals Nitroglycerin Transdermal System 0.2 mg/hr (10 cm2), For recall — FDA D-1236-2015
Failed Impurities/Degradation Specifications: failed specification for unknown impurity at the 24 month stability testing.
Class IIFDA: TerminatedKremers Urban Pharmaceuticals, Inc.
DrugJul 15, 2015
Apotex Enalapril maleate and hydrochlorothiazide tablets USP, 10/25 mg, 100-count bottle recall — FDA D-1215-2015
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
Class IIFDA: TerminatedApotex Inc.
DrugJul 15, 2015
American Health Packaging Clarithromycin tablets, USP 500mg recall — FDA D-1224-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Amlodipine besylate tablets, USP 2.5mg recall — FDA D-1218-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Zonisamide capsules, USP 100mg recall — FDA D-1230-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
Apotex Losartan potassium tablets USP, 25 mg, 90- count bottle recall — FDA D-1212-2015
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
Class IIFDA: TerminatedApotex Inc.
DrugJul 15, 2015
American Health Packaging Azithromycin tablets, USP 500mg recall — FDA D-1221-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 5mg recall — FDA D-1226-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
Hospira Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM recall — FDA D-1232-2015
Failed pH Specifications: 12 month stability testing
Class IIIFDA: TerminatedHospira Inc.
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 40mg recall — FDA D-1229-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
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.