DrugJul 15, 2015
American Health Packaging Azithromycin tablets, USP 250mg recall — FDA D-1223-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
10,690drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 297
10,690 detailed records are currently available in this category.
DrugJul 15, 2015
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, in 250mL VIAFLEX Plastic bags recall — FDA D-1208-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
American Health Packaging Amlodipine besylate tablets, USP 10 mg recall — FDA D-1220-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Famotidine tablets, USP 20mg recall — FDA D-1225-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 20mg recall — FDA D-1228-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
American Health Packaging Amlodipine besylate tablets, USP 5mg recall — FDA D-1219-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
Bupivacaine Hydrochloride Inj., USP, 0.5% (5 mg/mL), Preservative-Free, 30 mL Single Use recall — FDA D-1216-2015
Presence of Particulate Matter: Presence of free-floating and embedded iron oxide particles.
Class IFDA: TerminatedHospira Inc.
DrugJul 15, 2015
DEXTROSE 5% Dextrose Injection, USP, 250mL VIAFLEX Plastic bags recall — FDA D-1209-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
Lactated Ringers Injection, USP, 250mL VIAFELX Plastic bags recall — FDA D-1211-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
Teva Pharmaceuticals USA Adrucil recall — FDA D-1089-2015
Presence of Particulate Matter: Black particulate matter was identified as aggregate of silicone rubber pieces from a filler diaphragm and fluorouracil crystals.
Class IFDA: TerminatedTeva Pharmaceuticals USA
DrugJul 15, 2015
Apotex Losartan potassium tablets USP, 100 mg, 90-count bottle recall — FDA D-1213-2015
Failed Content Uniformity Specifications: The product may not meet the limit for blend uniformity specification.
Class IIFDA: TerminatedApotex Inc.
DrugJul 15, 2015
DEXTROSE 10% Dextrose Injection, USP, 250mL VIAFLEX Plastic bags recall — FDA D-1210-2015
Presence of Particulate Matter: Products recalled due to presence of particulate matter (metal)
Class IFDA: TerminatedBaxter Healthcare Corp.
DrugJul 15, 2015
BioComp Pharma Maximum Strength Analgesic Thera-Gesic Pain Relieving Creme Relief from recall — FDA D-1233-2015
Subpotent Drug: menthol and methyl salicylate below specification
Class IIIFDA: TerminatedBioComp Pharma, Inc.
DrugJul 15, 2015
Abrams Royal Pharmacy II CORTISOL-MC, 10mg CAP recall — FDA D-1231-2015
Failed Content Uniformity Specifications: Failed Uniformity of Dosage Units specifications.
Class IIIFDA: TerminatedAbrams Royal Pharmacy II, LLC
DrugJul 15, 2015
American Health Packaging Lisinopril tablets, USP 10mg recall — FDA D-1227-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 15, 2015
Apotex Losartan potassium tablets USP, 50 mg, 90-count bottle recall — FDA D-1214-2015
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 600mg recall — FDA D-1222-2015
CGMP Deviations: Firm did not adequately investigate customer complaints.
Class IIFDA: TerminatedAmerican Health Packaging
DrugJul 8, 2015
Lincare Morphine Sulfate, MORPHINE SULFATE 1000mg / NS 100mL, Qty: 1 50 mL Bag recall — FDA D-1200-2015
Lack of Assurance of Sterility: Sterility of product is not assured.
Class IIFDA: TerminatedLincare, Inc.
DrugJul 8, 2015
Lincare TPN 2:1, 200 ml Bags, Qty: 7, Base Formula NaCl 0.9%, Dextrose 70%, Trophamine 10% recall — FDA D-1158-2015
Lack of Assurance of Sterility: Sterility of product is not assured.
Class IIFDA: TerminatedLincare, Inc.
DrugJul 8, 2015
The Harvard Drug Group OXYCODONE HCl C-II Tablets, 5 mg USP, 100-count blister cards recall — FDA D-1150-2015
Superpotent Drug: Confirmed customer complaint of a single unit dose blister cavity containing 2 OXYCODONE HCl 5 mg tablets.
Class IIFDA: TerminatedThe Harvard Drug Group, LLC
DrugJul 8, 2015
Lincare Vancomycin, VANCOMYCIN 750mg / NS 100mL AccuFlo, Qty: 7 100 mL Bags recall — FDA D-1188-2015
Lack of Assurance of Sterility: Sterility of product is not assured.
Class IIFDA: TerminatedLincare, Inc.
DrugJul 8, 2015
Lincare Fluorouracil 1400mg / D5W 278mL Qty: 1 278 mL Bag recall — FDA D-1170-2015
Lack of Assurance of Sterility: Sterility of product is not assured.
Class IIFDA: TerminatedLincare, Inc.
DrugJul 8, 2015
Lincare Potassium Chloride, Dextrose 5% LR 1000 mL with 40mEq KCL, Qty: 1 1000 mL Bag recall — FDA D-1198-2015
Lack of Assurance of Sterility: Sterility of product is not assured.
Class IIFDA: TerminatedLincare, Inc.
DrugJul 8, 2015
Lincare TPN 3:1, 997 ml with lipids Bags, Qty: 7, Base Formula Dextrose 70%, Travasol 10% recall — FDA D-1155-2015
Lack of Assurance of Sterility: Sterility of product is not assured.
Class IIFDA: TerminatedLincare, 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.