DrugFeb 20, 2019
Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle recall — FDA D-0492-2019
Defective Container; complaints of leakage.
Class IIIFDA: TerminatedOxalis Labs
Latest records
Latest recalls — page 1288
The newest recall records with useful source details are listed here.
DrugFeb 20, 2019
Cardizem CD (diltiazem HCl) capsules, 180 mg recall — FDA D-0488-2019
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Class IIIFDA: TerminatedValeant Pharmaceuticals North America LLC
DrugFeb 20, 2019
Akorn COSOPT Ophthalmic Solution, USP recall — FDA D-0483-2019
Failed Stability Specifications: out of specification results for opalescence at 7 month stability study.
Class IIIFDA: TerminatedAkorn Inc.
DrugFeb 20, 2019
Tris Pharma infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg recall — FDA D-0494-2019
Superpotent Drug: recalled lots may have higher concentration of ibuprofen than amount labeled.
Class IIFDA: TerminatedTris Pharma Inc.
DrugFeb 20, 2019
Cardizem CD (diltiazem HCl) capsules, 300 mg recall — FDA D-0490-2019
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Class IIIFDA: TerminatedValeant Pharmaceuticals North America LLC
DrugFeb 20, 2019
Valeant Pharmaceuticals Diltiazem HCl CD capsules, 360 mg, 90-count bottles recall — FDA D-0491-2019
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Class IIIFDA: TerminatedValeant Pharmaceuticals North America LLC
DrugFeb 20, 2019
US Compounding LET Gel 4% recall — FDA D-0482-2019
Labeling: Incorrect or Missing Lot and/or Exp Date: Labels are missing lot and expiration date and are printed as Lot# YYYDDYY@XX with a Beyond Use Date: MM/DD/YYY.
Class IIFDA: TerminatedUS Compounding Inc.
DrugFeb 20, 2019
Avella of Deer Valley, Inc. Store 38 MAGnesium 2 gm sulfate, added to NS 50 mL, Sterile recall — FDA D-1000-2019
Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals information specific to the batch of the labeled…
Class IIFDA: TerminatedAvella of Deer Valley, Inc. Store 38
DrugFeb 20, 2019
Cardizem CD (diltiazem HCl) capsules, 120 mg recall — FDA D-0487-2019
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Class IIIFDA: TerminatedValeant Pharmaceuticals North America LLC
VehicleFeb 20, 2019
Volkswagen Group of shock absorber recall — NHTSA campaign 19V114000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2019 Q7, Q8, S5 Cabriolet, and S5 Sportback vehicles. The front shock absorber forks may develop cracks allowing the shock…
shock absorberVolkswagen Group of America, Inc.
VehicleFeb 20, 2019
Jetta frontal air bag recall — NHTSA campaign 19V110000
Volkswagen Group of America (Volkswagen) is recalling certain 2019 Jetta vehicles. An incorrect driver frontal airbag may have been installed during a service/repair visit.
frontal air bagVolkswagen Group of America, Inc.
Medical DeviceFeb 13, 2019
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Portex 1000 ml Sterile Water USP Pour Bottle¿¿¿¿ recall — FDA Z-0712-2019
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
Class IFDA: TerminatedMedex Cardio-Pulmonary Inc., d.b.a. Smiths Medical…
Medical DeviceFeb 13, 2019
Bard Medical Division SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray recall — FDA Z-0803-2019
potential for urine leakage around the vent on the vented sample port
Class IIFDA: TerminatedBard Medical Division
Medical DeviceFeb 13, 2019
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ recall — FDA Z-0713-2019
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
Class IFDA: TerminatedMedex Cardio-Pulmonary Inc., d.b.a. Smiths Medical…
Medical DeviceFeb 13, 2019
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Portex 350 ml Sterile Water Humidifier w/5psi recall — FDA Z-0710-2019
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
Class IFDA: TerminatedMedex Cardio-Pulmonary Inc., d.b.a. Smiths Medical…
Medical DeviceFeb 13, 2019
GE Healthcare Revolution CT systems with the SmartStep Option The system is intended for recall — FDA Z-0776-2019
On the Revolution CT systems equipped with the SmartStep Option, the Z location displayed on image annotation and on the gantry display may not be the actual location of the table and…
Class IIFDA: OngoingGE Healthcare, LLC
Medical DeviceFeb 13, 2019
Stryker Medical Division of Stryker Naera Hospital Bassinet, Model No. 4402 recall — FDA Z-0813-2019
It was identified that the volume of air inside the mattress may expand in regions of high altitude which may result in an unintended gap between the plateau of the inflated patient surface…
Class IIFDA: TerminatedStryker Medical Division of Stryker Corporation
Medical DeviceFeb 13, 2019
Angiotech Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm recall — FDA Z-0817-2019
Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
Class IIFDA: TerminatedAngiotech (Manan Medical Products, Inc.)
Medical DeviceFeb 13, 2019
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Portex 550 ml Sterile Water Humidifier w/5psi recall — FDA Z-0711-2019
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
Class IFDA: TerminatedMedex Cardio-Pulmonary Inc., d.b.a. Smiths Medical…
Medical DeviceFeb 13, 2019
Angiotech "J" Type Bone Marrow Needle 11ga x 10 cm - Product Usage: Manual surgical recall — FDA Z-0814-2019
Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
Class IIFDA: TerminatedAngiotech (Manan Medical Products, Inc.)
Medical DeviceFeb 13, 2019
ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800 recall — FDA Z-0802-2019
Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a…
Class IIFDA: TerminatedArjohuntleigh Magog
Medical DeviceFeb 13, 2019
BARD SureStep Foley Tray System Bardex I.C recall — FDA Z-0800-2019
Some SureStep" Foley Tray Systems with product catalog number A319418AM and lot number NGCT1929 contain vented sample ports that may have an increased likelihood of leaking urine from the…
Class IIFDA: OngoingBard Medical Division
Medical DeviceFeb 13, 2019
Angiotech J Type Bone Marrow Needle 13ga x 10 cm- Product Usage: Manual surgical instruments recall — FDA Z-0815-2019
Argon Medical has identified an internal manufacturing issue on the formation of the sterile seal on some of their blister trays for the Bone Marrow Biopsy Needle tray product line
Class IIFDA: TerminatedAngiotech (Manan Medical Products, Inc.)
Medical DeviceFeb 13, 2019
Radiometer ABL800 FLEX with Crea recall — FDA Z-0801-2019
From three incidents in Denmark and Sweden, comparison studies on patient blood samples carried out for quality assurance demonstrated that creatinine measurements as determined on…
Class IIFDA: TerminatedRadiometer America Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026184 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories