Medical DeviceSep 18, 2024
Medline convenience kits containing semi-rigid suction liners labeled as follows: a) AMB recall — FDA Z-3120-2024
XXX
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
September 2024 recalls — page 9
These records include useful source details for the selected month.
FoodSep 18, 2024
Reser's Fine Foods UPC 95515 04502, Amazon Fresh Fresh Classic Macaroni Salad recall — FDA F-1804-2024
Foreign material.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodSep 18, 2024
Reser's Fine Foods UPC 78742 02670, Walmart Original Freshness Guaranteed recall — FDA F-1806-2024
Foreign material.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodSep 18, 2024
Kester Foods Yummy Monkey Organics Real Movie Theater Popcorn, Made With recall — FDA F-1798-2024
Label declares butter and ghee but does not declare milk.
Class IIFDA: TerminatedKester Foods LLC
FoodSep 18, 2024
Orwaiian BDAY CAKE MOCHI CRUNCH packed in pink plastic pouch packaging recall — FDA F-1800-2024
Label has a Contains statement that is missing milk and coconut (tree nut) that are declared in the ingredients statement.
Class IIFDA: TerminatedOrwaiian LLC
FoodSep 18, 2024
Reser's Fine Foods UPC 71117 19084, Reser's American Classics Spicy Pickle Potato recall — FDA F-1802-2024
Foreign material.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodSep 18, 2024
Kester Foods Yummy Monkey Organics Butter & Yeast Popcorn, Made With recall — FDA F-1797-2024
Label declares butter and ghee but does not declare milk.
Class IIFDA: TerminatedKester Foods LLC
FoodSep 18, 2024
Reser's Fine Foods UPC 78742 12653, Walmart Original Freshness Guaranteed recall — FDA F-1805-2024
Foreign material.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodSep 18, 2024
Reser's Fine Foods UPC 71117 19063, Reser's American Classics Garden Pasta Salad recall — FDA F-1801-2024
Foreign material.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodSep 18, 2024
Reser's Fine Foods UPC 71117 14743, Reser s Rotisserie Chicken Salad Base 2lb recall — FDA F-1803-2024
Foreign material.
Class IIFDA: TerminatedReser's Fine Foods, Inc.
FoodSep 18, 2024
American Outdoor Products packaged in 0.5oz recall — FDA F-1807-2024
Elevated levels of lead
Class IIFDA: TerminatedAmerican Outdoor Products, Inc.
VehicleSep 18, 2024
BMW control module recall — NHTSA campaign 24V697000
BMW of North America (BMW) is recalling certain 2023-2024 X1, 2024-2025 X5, 2025 X6, 2023-2025 X7, 740i, 760i, 2024 XM, 530i, 540i, i7, 750e, X2, 2024-2025 i5, 2024 Rolls Royce Spectre,…
control moduleBMW of North America, LLC
DrugSep 18, 2024
Elevate Oral Care Just Right 5000, 1.1% Sodium Fluoride, Candy Apple Flavor, Net Wt. 3.4oz recall — FDA D-0658-2024
LABELING: LABEL MIX-UP.
Class IIIFDA: TerminatedElevate Oral Care
VehicleSep 13, 2024
Ford Maverick back over prevention software recall — NHTSA campaign 24V684000
Ford Motor Company (Ford) is recalling certain 2022-2024 Ford Maverick vehicles equipped with Connected Touch Radios (CTR). The rearview camera image may freeze when the vehicle is in…
back over prevention softwareFord Motor Company
VehicleSep 13, 2024
Ford Explorer hybrid propulsion system recall — NHTSA campaign 24V685000
Ford Motor Company (Ford) is recalling certain 2024 Ford Explorer vehicles equipped with 3.3L Hybrid engines. The 12-Volt battery cable may chafe against the Belt-integrated Starter Generat…
hybrid propulsion systemFord Motor Company
VehicleSep 13, 2024
F-150 lighting control module recall — NHTSA campaign 24V682000
Ford Motor Company (Ford) is recalling certain 2022 F-150 vehicles. The parking lights may flicker when the headlights are activated. As such, these vehicles fail to comply with the…
lighting control moduleFord Motor Company
VehicleSep 13, 2024
Tucson labels recall — NHTSA campaign 24V691000
Hyundai Motor America (Hyundai) is recalling certain 2025 Tucson vehicles. The glove box air bag warning label may be missing. As such, these vehicles fail to comply with the requirements…
labelsHyundai Motor America
VehicleSep 12, 2024
GMC Canyon headlights recall — NHTSA campaign 24V673000
General Motors, LLC (GM) is recalling certain 2024 GMC Canyon vehicles. The headlights may flicker while driving and while the vehicle is in park. As such, these vehicles fail to comply…
headlightsGeneral Motors, LLC
VehicleSep 12, 2024
General Motors lamp recall — NHTSA campaign 24V674000
General Motors, LLC (GM) is recalling certain 2023 Chevrolet Silverado 1500, GMC Sierra 1500, 2023-2024 Chevrolet Tahoe, Suburban, GMC Yukon, Yukon XL, Cadillac Escalade, and Escalade ESV…
lampGeneral Motors, LLC
VehicleSep 12, 2024
Jeep Wrangler camera recall — NHTSA campaign 24V676000
Chrysler (FCA US, LLC) is recalling certain 2018-2024 Jeep Wrangler vehicles. The wiring harness for the rearview camera and the center brake light may short circuit, which can disable the…
cameraChrysler (FCA US, LLC)
Medical DeviceSep 11, 2024
W L Gore & Associates Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the recall — FDA Z-2946-2024
Due to packaging defects, sterility assurance and heparin activity may be compromised.
Class IIFDA: OngoingW L Gore & Associates, Inc.
Medical DeviceSep 11, 2024
Abiomed Impella 5.5 with SmartAssist Set, US recall — FDA Z-2963-2024
A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.)…
Class IIFDA: OngoingAbiomed, Inc.
Medical DeviceSep 11, 2024
Abiomed Impella 5.5 Set AU recall — FDA Z-2968-2024
A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.)…
Class IIFDA: OngoingAbiomed, Inc.
Medical DeviceSep 11, 2024
Abiomed Pump 371 14F LT CMR Set recall — FDA Z-2959-2024
A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.)…
Class IIFDA: OngoingAbiomed, Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.