FoodAug 4, 2021
RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902 recall — FDA F-0805-2021
Lack of functioning Temperature Indicating Devices in retorts
Class IIFDA: TerminatedRandall Foods, Inc.
Latest records
Latest recalls — page 842
The newest recall records with useful source details are listed here.
FoodAug 4, 2021
Old Souls Farms 2 lbs, and 5 oz clamshells - 1oz 18 per case, 5oz 6 per case recall — FDA F-0866-2021
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Class IFDA: TerminatedOld Souls Farms LLC
FoodAug 4, 2021
RANDALL KIDNEY BEANS 48OZ glass jars UPC 070095000308 recall — FDA F-0801-2021
Lack of functioning Temperature Indicating Devices in retorts
Class IIFDA: TerminatedRandall Foods, Inc.
FoodAug 4, 2021
Old Souls Farms 5oz 6 per case bulk bags - 1lb is 3 per case, 10lbs 1 per recall — FDA F-0865-2021
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Class IFDA: TerminatedOld Souls Farms LLC
FoodAug 4, 2021
Amys Kitchen Amy's Bowls, Tortilla Casserole & Black Beans recall — FDA F-0797-2021
Potential of pieces of rubber gasket from production equipment in Tortilla Casserole Bowl.
Class IIFDA: TerminatedAmys Kitchen Inc.
FoodAug 4, 2021
BLUE ROBINS Choujuki White Bread 6 slices: Net Wt recall — FDA F-0807-2021
Internal label review found that their labeling did not properly declare milk (sub ingredient of margarine) or as an allergen
Class IIFDA: TerminatedBLUE ROBINS Inc.
FoodAug 4, 2021
Old Souls Farms 2lbs, and living oz are packed in clamshells - 1oz 18 per recall — FDA F-0861-2021
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Class IFDA: TerminatedOld Souls Farms LLC
FoodAug 4, 2021
Rich Products f'real Made to Order Shake Base - 8 fl oz recall — FDA F-0818-2021
Shake base contains undeclare milk due to wrong outer-label stating product is Smoothie Base.
Class IIFDA: TerminatedRich Products Corp
FoodAug 4, 2021
RANDALL NAVY BEANS 48OZ glass jars UPC 070095000506 recall — FDA F-0802-2021
Lack of functioning Temperature Indicating Devices in retorts
Class IIFDA: TerminatedRandall Foods, Inc.
FoodAug 4, 2021
Dole Fresh Picked-Emballes frais Blueberries/Bleuets: Packed recall — FDA F-0796-2021
Canadian Food Inspection Agency tested blueberries and found Cyclospora cayetanensis.
Class IIFDA: TerminatedDole Fresh Fruit Company
FoodAug 4, 2021
RANDALL GREAT NORTHERN BEANS 48OZ glass jar UPC 070095000100 recall — FDA F-0798-2021
Lack of functioning Temperature Indicating Devices in retorts
Class IIFDA: TerminatedRandall Foods, Inc.
FoodAug 4, 2021
Old Souls Farms 5 oz, Living Heads clamshells - 1oz 18 per case, 5oz 6 per recall — FDA F-0864-2021
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Class IFDA: TerminatedOld Souls Farms LLC
FoodAug 4, 2021
RANDALL MIXED BEANS 48OZ glass jars UPC 070095000407 recall — FDA F-0800-2021
Lack of functioning Temperature Indicating Devices in retorts
Class IIFDA: TerminatedRandall Foods, Inc.
FoodAug 4, 2021
Old Souls Farms 5oz 6 per case bulk bags - 1lb is 3 per case, 10lbs 1 per recall — FDA F-0863-2021
Positive rainwater test for Listeria monocytogenes. The rainwater came in contact with product.
Class IFDA: TerminatedOld Souls Farms LLC
VehicleAug 2, 2021
BMW engine recall — NHTSA campaign 21V598000
BMW of North America, LLC (BMW) is recalling certain 2020 M340i, M340i xDrive, 540i, 540i xDrive, X3 M40i, 2020-2021 X4 M40i, 745Le xDrive, 2019-2021 Z4 M40i, and 2020-2021 Toyota Supra…
engineBMW of North America, LLC
VehicleJul 29, 2021
General Motors control module software recall — NHTSA campaign 21V579000
General Motors, LLC (GM) is recalling certain 2021 Chevrolet Tahoe and GMC Yukon vehicles. Dealer service technicians may have calibrated the brake system incorrectly, affecting Electronic…
control module softwareGeneral Motors, LLC
VehicleJul 29, 2021
Subaru of fuel pump recall — NHTSA campaign 21V587000
Subaru of America, Inc. (Subaru) is recalling certain 2019-2020 Ascent, 2018 Forester, 2018-2020 Impreza, Legacy, Outback, 2018-2019 BRZ, WRX, and Toyota 86 vehicles. The low-pressure fuel…
fuel pumpSubaru of America, Inc.
Medical DeviceJul 28, 2021
Dutch Ophthalmic USA Illuminated Stepped Laser Probe Curved-for use in combination with 23G recall — FDA Z-2097-2021
Barcode label extended expiration date. Barcode located at the short side of the outer box shows 2025-10-27 when scanned, while the correct expiry date is 2024-10-01
Class IIFDA: OngoingDutch Ophthalmic USA, Inc.
Medical DeviceJul 28, 2021
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog recall — FDA Z-2133-2021
Risk of edge-loading and premature prosthesis wear is possible in a specific subset of patients with certain implant configurations and surgical implant positioning.
Class IIFDA: OngoingExactech, Inc.
Medical DeviceJul 28, 2021
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog recall — FDA Z-2114-2021
Risk of edge-loading and premature prosthesis wear is possible in a specific subset of patients with certain implant configurations and surgical implant positioning.
Class IIFDA: OngoingExactech, Inc.
Medical DeviceJul 28, 2021
Mckesson Medical-Surgical Inc. Corporate Office ANCILLARY ADULT 140-DOSE CONVENIENCE KIT recall — FDA Z-2081-2021
Two unsuitable 3mL syringes with conventional needles for vaccine administration included in some Moderna 140 Ancillary Convenience Kits.
Class IIFDA: TerminatedMckesson Medical-Surgical Inc. Corporate Office
Medical DeviceJul 28, 2021
Fresenius Medical Care Holdings 050-95012 Sterile Stay Safe Cap The Indications for recall — FDA Z-2090-2021
Exposed to freezing temperatures due to refrigerated truck malfunctions
Class IIFDA: TerminatedFresenius Medical Care Holdings, Inc.
Medical DeviceJul 28, 2021
Gentherm Medical Hemotherm CE Dual Reservoir Cooler/Heater, Model 400CE, 115V Model, part recall — FDA Z-2092-2021
There is a potential risk of device contamination and patient infection associated with the device because of the potential for organisms (including Nontuberculous mycobacteria NTM) to grow…
Class IIFDA: TerminatedGentherm Medical, LLC
Medical DeviceJul 28, 2021
Cell Marque, RabMAb,CD17, c-kit (YR145) Rabbit Monoclonal Primary Antibody, REF: 117R-18 recall — FDA Z-2105-2021
Product distributed for use as an In-vitro Diagnostics without FDA clearance
Class IIFDA: TerminatedCell Marque Corporation
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026111 records · 4 categoriesSeptember 2026364 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