DrugFeb 17, 2016
Pramipexole Dihydrochloride Tablets 0.125 mg, 90 Ct Bottles recall — FDA D-0653-2016
Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5 mg tablet.
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
10,690drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 274
10,690 detailed records are currently available in this category.
DrugFeb 10, 2016
Lyrica (pregabalin) capsules, 75 mg, 90-count bottle recall — FDA D-0649-2016
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
Class IIFDA: TerminatedPfizer Inc.
DrugFeb 10, 2016
Lyrica (pregabalin) capsules, 50 mg, 90-count bottle recall — FDA D-0648-2016
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
Class IIFDA: TerminatedPfizer Inc.
DrugFeb 3, 2016
Sentara Enterprises Dextrose-NaCl (D5-1/2NS) in NS recall — FDA D-0620-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Perrigo Company PLC Guaifenesin DM Cherry liquid recall — FDA D-0587-2016
Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
Class IIFDA: TerminatedPerrigo Company PLC
DrugFeb 3, 2016
Sentara Enterprises Lactated Ringers recall — FDA D-0636-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises HYDROMORPHONE HCL, Packaged as a) 2.5MG in 1ML Syringes, b) 150MG in recall — FDA D-0625-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Cyclopentolate Hydrochloride Ophthalmic Solution USP, 1% recall — FDA D-0645-2016
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Class IIIFDA: TerminatedBausch & Lomb, Inc.
DrugFeb 3, 2016
Sentara Enterprises CEFAZOLIN, Packaged as a) 625MG in 6.2ML Syringes, b) 2GM in 20ML recall — FDA D-0615-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises Milrinone in 0.45% NS, Packaged as a) 52MG in 65ML Homepumps, b) 80MG in recall — FDA D-0616-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises PENICILLIN in D5W, Packaged as a)36MU in 360ML Homepumps and b) 51MU in recall — FDA D-0632-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises Invanz (ertapenem) Injection Recon Soln in NS, Packaged as a) 500MG in recall — FDA D-0628-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises SOD CHLORIDE (Sodium Chloride) recall — FDA D-0613-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises GANCICLOVIR in NS, Packaged as a) 320MG in 64ML Homepumps and b) 2440MG recall — FDA D-0626-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Tropicamide Ophthalmic Solution USP, 0.5% recall — FDA D-0646-2016
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Class IIIFDA: TerminatedBausch & Lomb, Inc.
DrugFeb 3, 2016
Perrigo Company PLC Guaifenesin Grape liquid 100 mg/5 mL recall — FDA D-0586-2016
Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
Class IIFDA: TerminatedPerrigo Company PLC
DrugFeb 3, 2016
Amerisource Health Services Levofloxacin Tablets USP, 500 mg recall — FDA D-0610-2016
Failed Dissolution Specifications: Unexplained low out of specification results for dissolution.
Class IIFDA: TerminatedAmerisource Health Services
DrugFeb 3, 2016
Sentara Enterprises ZOSYN (pipericillin/tazobactam) in NS, Packaged as a) 3.375GM in 50ML recall — FDA D-0630-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises VANCOMYCIN HCL, Packaged as: a) 600MG in 120ML Homepumps, b) 750MG in recall — FDA D-0623-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Tropicamide Ophthalmic Solution USP, 1% recall — FDA D-0647-2016
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Class IIIFDA: TerminatedBausch & Lomb, Inc.
DrugFeb 3, 2016
Sentara Enterprises DOBUTAMINE HCL in D5W, Packaged as a) 240MG in 60ML Homepumps and b) recall — FDA D-0622-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises GENTAMICIN, Packaged as a) 70MG in 70ML Homepumps, b) 80MG in 80ML recall — FDA D-0641-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises INTRALIPID (fat emulsion) recall — FDA D-0618-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
DrugFeb 3, 2016
Sentara Enterprises Parenteral Amino Acid Infusion 10% recall — FDA D-0614-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class IIFDA: TerminatedSentara Enterprises
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.