FoodFeb 26, 2020
CSM Bakery Products 32 lb recall — FDA F-0730-2020
Pieces of plastic polymer were introduced into the sugar system.
Class IIFDA: TerminatedCSM Bakery Products
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 151
Records are ordered by the best available source date.
FoodFeb 26, 2020
Don Lee Farms Chipotle Black Bean Burger 12 pack/3Lbs recall — FDA F-0768-2020
An ingredient used in the manufacture of finished product was discovered to have been grown using unapproved herbicide.
Class IIIFDA: TerminatedDon Lee Farms
FoodFeb 26, 2020
CSM Bakery Products 14 lb recall — FDA F-0726-2020
Pieces of plastic polymer were introduced into the sugar system.
Class IIFDA: TerminatedCSM Bakery Products
FoodFeb 26, 2020
CSM Bakery Products 43 lb recall — FDA F-0723-2020
Pieces of plastic polymer were introduced into the sugar system.
Class IIFDA: TerminatedCSM Bakery Products
FoodFeb 26, 2020
Suja Life 12 oz recall — FDA F-0770-2020
Firm was notified by supplier of an unapproved herbicide in raw material, flax, that was used in their juice product.
Class IIFDA: TerminatedSuja Life LLC
FoodFeb 26, 2020
CSM Bakery Products 40 lb recall — FDA F-0722-2020
Pieces of plastic polymer were introduced into the sugar system.
Class IIFDA: TerminatedCSM Bakery Products
FoodFeb 26, 2020
The Honest Stand Hungry Root Dairy free Garlic Parm sauce, Packaged in 9 oz recall — FDA F-0711-2020
Undeclared Allergen: Product contains both cashews and almonds, but only almonds were labeled on the physical product. Both allergens were labeled on the electronic ingredient statement…
Class IFDA: TerminatedThe Honest Stand
FoodFeb 26, 2020
CSM Bakery Products 35 lb recall — FDA F-0728-2020
Pieces of plastic polymer were introduced into the sugar system.
Class IIFDA: TerminatedCSM Bakery Products
FoodFeb 26, 2020
New Seasons Market Vegetarian Lasagna With Gluten-Free Pasta, New Seasons Market recall — FDA F-0713-2020
Undeclared Soy. BBQ sauce was inadvertently used instead of Marinara sauce and BBQ sauce contains soy. The Vegetarian Lasagna finished product label does not declare soy.
Class IIFDA: TerminatedNew Seasons Market LLC
DrugFeb 26, 2020
Memantine Hydrochloride Extended-release Capsules, 28mg recall — FDA D-0844-2020
Failed Dissolution Specifications: High out of specification result observed at stability studies.
Class IIIFDA: TerminatedThe Harvard Drug Group
DrugFeb 26, 2020
Glycopyrrolate Injection, USP 4 mg per 20 mL (0.2 mg/mL), 20 mL Multiple Dose Vial recall — FDA D-0853-2020
Failed Impurities/Degradation Specifications: elevated levels of Benzaldehyde impurity was found in investigative samples (retain samples).
Class IIIFDA: TerminatedAuroMedics Pharma LLC
DrugFeb 26, 2020
Teva Pharmaceuticals USA Tramadol Hydrochloride Tablets USP CIV, 50 mg recall — FDA D-0851-2020
Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored…
Class IIIFDA: TerminatedTeva Pharmaceuticals USA
DrugFeb 26, 2020
American Health Packaging Desmopressin Acetate Tablets, 0.2 mg, 30 tablets recall — FDA D-0849-2020
GMP Deviations: Product bottle may be absent of desiccant.
Class IIFDA: TerminatedAmerican Health Packaging
DrugFeb 26, 2020
American Health Packaging Desmopressin Acetate Tablets, 0.1 mg, 30 tablets recall — FDA D-0848-2020
GMP Deviations: Product bottle may be absent of desiccant.
Class IIFDA: TerminatedAmerican Health Packaging
VehicleFeb 21, 2020
Ford headlights recall — NHTSA campaign 20V097000
Ford Motor Company (Ford) is recalling certain 2018-2020 F-150 trucks equipped with high series LED headlamps with Autolamp (On/Off) functionality. The Daytime Running Lamps (DRL) may…
headlightsFord Motor Company
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME recall — FDA Z-1212-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers recall — FDA Z-1224-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220 recall — FDA Z-1217-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Philips VesselNavigator application used with Philips Azurion (Azurion 7 Series) Software recall — FDA Z-1145-2020
Due to a software defect, when a digital subtraction angiography (DSA) is exported to the VesselNavigator application, the DSA is displayed without subtraction.
Class IIFDA: TerminatedPhilips North America, LLC
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers recall — FDA Z-1222-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
TELEFLEX MEDICAL HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote recall — FDA Z-1113-2020
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column…
Class IFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceFeb 19, 2020
Respironics V680 Ventilator, Service # 850011, (OUS Only) recall — FDA Z-1155-2020
Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchcreen,…
Class IIFDA: OngoingRespironics California, LLC
Medical DeviceFeb 19, 2020
Arrow International EPIDURAL CATHETERIZATION KIT, Product Code MTO-09903-KU recall — FDA Z-1210-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
TELEFLEX MEDICAL HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port recall — FDA Z-1115-2020
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column…
Class IFDA: TerminatedTELEFLEX MEDICAL 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.