FoodSep 30, 2020
Frito-Lay 28 count Classic Cube Mix cube box UPC 28400 15586 1 recall — FDA F-1529-2020
May contain undeclared milk
Class IFDA: TerminatedFrito-Lay, Inc.
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 43
Records are ordered by the best available source date.
FoodSep 30, 2020
Freshouse Produce Wegmans Valencia Oranges, 4lb mesh bag, UPC 77890 52363 recall — FDA F-1537-2020
The firm received positive Environmental sampling results for Listeria monocytogenes.
Class IIFDA: OngoingFreshouse Produce
FoodSep 30, 2020
Gilster-Mary Lee Microwave popcorn packaged in the following ways: 1) Full recall — FDA F-1544-2020
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
Class IIFDA: TerminatedGilster-Mary Lee Corp.
DrugSep 30, 2020
Incredible Products Gelbac T Antibacterial Hand Gel (ethyl alcohol 80%), Kills 99.9% recall — FDA D-1587-2020
Chemical Contamination: Product contains methanol as an active ingredient and is sub-potent for ethanol.
Class IFDA: TerminatedIncredible Products, SA de CV
DrugSep 30, 2020
Nanomateriales Sa De Cv Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) recall — FDA D-1593-2020
GMP Deviations: Potential to contain 1-propanol.
Class IIFDA: TerminatedNanomateriales Sa De Cv
DrugSep 30, 2020
Nanomateriales Sa De Cv Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) recall — FDA D-1592-2020
GMP Deviations: Potential to contain 1-propanol.
Class IIFDA: TerminatedNanomateriales Sa De Cv
DrugSep 30, 2020
CORGIOMED Leafree Instant Hand Sanitizer Aloe Vera (ethyl alcohol 70% v/v), Kills 99.99% recall — FDA D-1586-2020
Marketed without an Approved NDA/ANDA; product labeled as Edible Alcohol rendering the product an unapproved new drug and misbranded.
Class IFDA: TerminatedCORGIOMED LLC
DrugSep 30, 2020
Preferred Pharmaceuticals Nature-Throid, 3/4 Grain (48.75 mg) Thyroid U.S.P. 3/4 gr. recall — FDA D-1622-2020
CGMP Deviations
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
DrugSep 30, 2020
AJR TRADING bio aaa Alcohol en Gel Antibacterial, Alcohol al 70% Cont recall — FDA D-1620-2020
CGMP Deviations: Product manufactured in a facility where methanol was found in other distributed lots of product.
Class IIFDA: TerminatedAJR TRADING LLC
DrugSep 30, 2020
Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations recall — FDA D-1594-2020
Defective Delivery System: Sustained trend of failure to dispense complaints.
Class IIFDA: TerminatedPerrigo Company PLC
DrugSep 30, 2020
The Protein Shoppe Red-E Tablet, Proprietary Blend 3000 mg** recall — FDA D-1595-2020
Marketed Without An Approved NDA/ANDA: product found to be tainted with sildenafil, an FDA approved drug for the treatment of male erectile dysfunction, making this an unapproved drug fro…
Class IFDA: TerminatedThe Protein Shoppe
DrugSep 30, 2020
Preferred Pharmaceuticals Nature-Throid, 1.5 Grain, (97.5 mg) recall — FDA D-1624-2020
CGMP Deviations
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
DrugSep 30, 2020
GRUPO YACANA MEXICO SAS DE CV Yacana Alcohol Antiseptic 70% Topical Solution 8.5 oz recall — FDA D-1590-2020
cGMP Deviations
Class IIFDA: TerminatedGRUPO YACANA MEXICO SAS DE CV
DrugSep 30, 2020
Preferred Pharmaceuticals Nature-Throid, 1/2 Grain, 32.5 mg recall — FDA D-1621-2020
CGMP Deviations
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
DrugSep 30, 2020
Preferred Pharmaceuticals Nature-Throid, 1 Grain, 65 mg recall — FDA D-1623-2020
CGMP Deviations
Class IIFDA: TerminatedPreferred Pharmaceuticals, Inc.
VehicleSep 30, 2020
Model Y exterior lighting recall — NHTSA campaign 20V609000
Tesla, Inc. (Tesla) is recalling certain 2020 Model Y vehicles equipped with a global rear lamp and tow package configuration. A software error prevents the illumination of trailer brake…
exterior lightingTesla, Inc.
VehicleSep 30, 2020
BMW camera recall — NHTSA campaign 20V598000
BMW of North America, LLC (BMW) is recalling certain 2020-2021 X3 sDrive 30i, X3 xDrive 30i, X3M 40i, X3 xDrive 30e, X4 xDrive 30i, X4M 40i, 530i, 540i, 540i xDrive, M550i xDrive, M5, 550e,…
cameraBMW of North America, LLC
VehicleSep 30, 2020
BMW traction battery recall — NHTSA campaign 20V601000
BMW of North America, LLC (BMW) is recalling certain 2020-2021 530e, 530e xDrive, 530e iPerformance and X3 xDrive30e and MINI Cooper Countryman All4 SE, 2020 BMW i8, and 2021 330e, 330e…
traction batteryBMW of North America, LLC
VehicleSep 24, 2020
General Motors service brakes recall — NHTSA campaign 20V588000
General Motors LLC (GM) is recalling certain 2020 Chevrolet Corvette and Cadillac CT4, CT5 and XT4, 2021 Chevrolet Trailblazer, and 2020-2021 Buick Encore GX vehicles. Sensor connection…
service brakesGeneral Motors LLC
VehicleSep 24, 2020
Chrysler seat belts recall — NHTSA campaign 20V580000
Chrysler (FCA US LLC) is recalling certain 2019 Jeep Wrangler and Ram 2500, 2019-2020 Ram 1500 and 2020 Jeep Gladiator vehicles. In the event of a crash, a front seat belt retractor may not…
seat beltsChrysler (FCA US LLC)
Medical DeviceSep 23, 2020
Cook Medical Universa Soft Ureteral Stent Sets-5 FR 26 cm Reference part Number: UFH-526 recall — FDA Z-2971-2020
Universa Soft Ureteral Stent Sets were incorrectly placed in the outer boxes labeled as Universa Firm Ureteral Stent Set ;pouch label reflects the packaged product.
Class IIFDA: TerminatedCook Inc.
Medical DeviceSep 23, 2020
Boston Scientific WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent) recall — FDA Z-2958-2020
Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices labeled as WallFlexTM Biliary RX Fully Covered Stent System RMV 10x60mm device
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceSep 23, 2020
RANDOX LABORATORIES AM1054 Randox Ammonia (NH3), Enzymatic UV Method For the quantitative in recall — FDA Z-2966-2020
Randox Ammonia reagents are being recalled from the field due to a positive bias of up to 140¿mol/l being observed on patient samples.
Class IIFDA: TerminatedRANDOX LABORATORIES, LTD.
Medical DeviceSep 23, 2020
Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK, Catalog Number recall — FDA Z-2960-2020
Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) sensor connector backwards, preventing the crimped wire from locking into the…
Class IIFDA: TerminatedTerumo Cardiovascular Systems Corporation
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.