DrugAug 5, 2020
Allergan PLC Skin Medica Acne System, Contains: Purifying Foaming Wash recall — FDA D-1410-2020
SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
Class IIIFDA: TerminatedAllergan PLC
Monthly breakdown
2020 recalls by month
Select a month to review the recall records reported during that period.
December 2020315 records · 4 categoriesNovember 2020241 records · 4 categoriesOctober 2020416 records · 4 categoriesSeptember 2020371 records · 4 categoriesAugust 2020245 records · 4 categoriesJuly 2020442 records · 4 categoriesJune 2020342 records · 4 categoriesMay 2020315 records · 4 categoriesApril 2020422 records · 4 categoriesMarch 2020368 records · 4 categoriesFebruary 2020551 records · 4 categoriesJanuary 2020224 records · 4 categories
2020 recalls — page 67
Records are ordered by the best available source date.
DrugAug 5, 2020
Lisinopril Tablets USP, 10 mg, 1000 count bottles recall — FDA D-1413-2020
Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril Tablets USP, 10mg
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugAug 5, 2020
MasterPharm Formula 82M recall — FDA D-1424-2020
Lack of Processing Controls (lack of assurance of conformity to specifications).
Class IIFDA: TerminatedMasterPharm LLC
VehicleAug 5, 2020
Forte axle shaft recall — NHTSA campaign 20V459000
Kia Motors America (Kia) is recalling certain 2019 Forte vehicles. The left front axle driveshaft may not have been heat-treated, which can cause it to break.
axle shaftKia Motors America
VehicleJul 30, 2020
General Motors curtain air bag inflator recall — NHTSA campaign 20V446000
General Motors, LLC. (GM) is recalling certain 2020 Buick Enclave, Cadillac XT5 and XT6, Chevrolet Blazer, Silverado 1500, 2500 and 3500 and Traverse and GMC Acadia and Sierra 1500, 2500…
curtain air bag inflatorGeneral Motors LLC
Medical DeviceJul 29, 2020
Becton Dickinson & Company SafeStep Huber Needle Set recall — FDA Z-2671-2020
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to…
Class IIFDA: TerminatedBecton Dickinson & Company
Medical DeviceJul 29, 2020
Philips IntelliVue MX700 patient monitor, model no. 865241 recall — FDA Z-2697-2020
Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding…
Class IIFDA: TerminatedPhilips North America, LLC
Medical DeviceJul 29, 2020
Becton Dickinson & Company PowerLoc MAX Power Injectable Infusion Set with GuardIVa recall — FDA Z-2663-2020
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to…
Class IIFDA: TerminatedBecton Dickinson & Company
Medical DeviceJul 29, 2020
Boston Scientific Ablation Galil Technology, IceFORCE 2.1 CX Needle Cryoablation Needle recall — FDA Z-2677-2020
The needle surface deteriorated due to unexpected electrolysis during procedure.
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJul 29, 2020
Boston Scientific Ablation Galil Technology, Three IceFORCE 2.1 Prostate Cyroablation Kit recall — FDA Z-2681-2020
The needle surface deteriorated due to unexpected electrolysis during procedure.
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJul 29, 2020
Boston Scientific Ablation Galil Technology, IcePearl 2.1 CX 90 Cyroablation Needles recall — FDA Z-2682-2020
The needle surface deteriorated due to unexpected electrolysis during procedure.
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJul 29, 2020
Siemens Medical Solutions USA syngo.via RT Image Suite with software versions syngo.via VB30 recall — FDA Z-2688-2020
If the user modifies for any reason (e.g. reduction of artifacts) the original image orientation of a standard MR protocol to acquire images in a different orientation for further…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceJul 29, 2020
Becton Dickinson & Company SafeStep Huber Needle Set AllPoints Port Access System recall — FDA Z-2664-2020
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to…
Class IIFDA: TerminatedBecton Dickinson & Company
Medical DeviceJul 29, 2020
Carefusion 2200 Thora-Para 5 Fr Non-Valved Catheter Drainage Tray recall — FDA Z-2646-2020
The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.
Class IIFDA: TerminatedCarefusion 2200 Inc.
Medical DeviceJul 29, 2020
Medtronic Sofamor Danek USA Accurian RF Ablation, Cannula pk, Accurian, 100mm, 18G, 10mm, CS recall — FDA Z-2690-2020
Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.
Class IIFDA: TerminatedMedtronic Sofamor Danek USA Inc.
Medical DeviceJul 29, 2020
EHOB Expansion Control Overlay, Item No. 1004EC - Product Usage: The EHOB WAFFLE Overlay is recall — FDA Z-2640-2020
QC inspection observed that a portion of the lot may have been contaminated with blood.
Class IIFDA: TerminatedEHOB, Inc.
Medical DeviceJul 29, 2020
Shanghai United Imaging Healthcare Co Computed Tomography X-ray System, Model: uCT 550 recall — FDA Z-2641-2020
Two issues were identified with the computed tomography x-ray system including a service function which may cause false marking of a bad channel resulting in ring artifacts, and potential…
Class IIFDA: OngoingShanghai United Imaging Healthcare Co., Ltd.
Medical DeviceJul 29, 2020
Carefusion 2200 Safe-T 8 Fr Thora-Para Tray With 8 Fr recall — FDA Z-2655-2020
The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.
Class IIFDA: TerminatedCarefusion 2200 Inc.
Medical DeviceJul 29, 2020
Becton Dickinson & Company SafeStep Huber Needle Set myPICK Port Access Kit recall — FDA Z-2665-2020
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to…
Class IIFDA: TerminatedBecton Dickinson & Company
Medical DeviceJul 29, 2020
Carefusion 2200 Safe-T 5 Fr Thora-Para Tray With 5 Fr recall — FDA Z-2658-2020
The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.
Class IIFDA: TerminatedCarefusion 2200 Inc.
Medical DeviceJul 29, 2020
Philips IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00 recall — FDA Z-2689-2020
The device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and display of gas levels and generating one or more technical or INOP alarms.
Class IIFDA: OngoingPhilips North America, LLC
Medical DeviceJul 29, 2020
Medtronic Sofamor Danek USA Accurian RF Ablation, Cannula pk, Accurian, 150mm, 18G, 10mm, CS recall — FDA Z-2691-2020
Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.
Class IIFDA: TerminatedMedtronic Sofamor Danek USA Inc.
Medical DeviceJul 29, 2020
Boston Scientific Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle recall — FDA Z-2674-2020
The needle surface deteriorated due to unexpected electrolysis during procedure.
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJul 29, 2020
Medtronic Sofamor Danek USA Accurian RF Ablation, Cannula pk, Accurian, 100mm, 20G, 10mm, CS recall — FDA Z-2692-2020
Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.
Class IIFDA: TerminatedMedtronic Sofamor Danek USA Inc.
About the 2020 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.