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.
Monthly breakdown
2021 recalls by month
Select a month to review the recall records reported during that period.
December 2021194 records · 4 categoriesNovember 2021210 records · 4 categoriesOctober 2021342 records · 4 categoriesSeptember 2021300 records · 4 categoriesAugust 2021279 records · 4 categoriesJuly 2021251 records · 4 categoriesJune 2021361 records · 4 categoriesMay 2021226 records · 4 categoriesApril 2021279 records · 4 categoriesMarch 2021241 records · 4 categoriesFebruary 2021320 records · 4 categoriesJanuary 2021226 records · 4 categories
2021 recalls — page 56
Records are ordered by the best available source date.
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
Medical DeviceJul 28, 2021
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog recall — FDA Z-2116-2021
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-2122-2021
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
Mediana Co AVSM3 SNF, Vital Signs Monitor The monitor is intended to be used to monitor recall — FDA Z-2096-2021
In some cases the equipment fails to power up and/or key or button unresponsive or not working.
Class IIFDA: TerminatedMediana Co., Ltd.
Medical DeviceJul 28, 2021
Fresenius Medical Care Holdings The MTS Set is a single-use, sterile (EO), non-pyrogenic recall — FDA Z-2089-2021
Exposed to freezing temperatures due to refrigerated truck malfunctions
Class IIFDA: TerminatedFresenius Medical Care Holdings, Inc.
Medical DeviceJul 28, 2021
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog recall — FDA Z-2125-2021
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
Fresenius Medical Care Holdings NaturaLyte Dry Bicarbonate Concentrate is composed of sodium recall — FDA Z-2087-2021
Exposed to freezing temperatures due to refrigerated truck malfunctions
Class IIFDA: TerminatedFresenius Medical Care Holdings, Inc.
Medical DeviceJul 28, 2021
Cardinal Health 200 Infant Heel Warmer without Attachment Tab, Nonsterile, Active Product recall — FDA Z-2095-2021
A caution statement is being added to remind the user to activate away from face and infant as reports of pack rupture or leaking during activation may resulting in the contents splashing…
Class IIFDA: TerminatedCardinal Health 200, LLC
Medical DeviceJul 28, 2021
Respironics California Philips Respironics V60 Ventilator with Software Versions 3.00 and recall — FDA Z-2073-2021
It has been identified that ventilators equipped with High Flow Therapy (Software Versions 3.00 and 3.10), that includes a designed safety mechanism that limits the amount of pressure that…
Class IFDA: OngoingRespironics California, LLC
Medical DeviceJul 28, 2021
Caption Health Version: 1.2.0 (1.2.0+85ela410) Caption Health, Caption AI, Ultrasound recall — FDA Z-2111-2021
The firm is aware of a issue with ultrasound software that results in unintended video frames being included. This could lead to an incorrect automated ejection fraction (AutoEF) and image…
Class IIFDA: TerminatedCaption Health
Medical DeviceJul 28, 2021
Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog recall — FDA Z-2120-2021
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.
About the 2021 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.