Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

5526–5550 of 7463

SevereFDA (Devices)·Z-0143-2023·2022-11-09
Hillrom WatchCare Incontinence System Recalled for Radio Frequency Interference
Baxter Healthcare recalls the Hillrom WatchCare Incontinence Management System for Progressa Bed due to potential radio frequency emissions that may interfere with other medical devices including telemetry monitors and infusion pumps.
Product
Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Progressa Bed, Product Code/Part Number P00697903.
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-0109-2023·2022-11-09
Joan of Arc Peppercorn Cheese Wheels Recalled for Listeria Contamination
Old Europe Cheese is recalling Joan of Arc 2.2 lb peppercorn wheel cheese due to potential Listeria monocytogenes contamination. Affected products have best-by dates from September 28 to December 14, 2022.
Product
JOAN OF ARC 2.2 lb Joan of Arc Peppercorn Wheel no UPC
Category
Food
Distribution
25 states
SevereFDA (Food)·F-0112-2023·2022-11-09
Baked Brie Cheese Recalled for Potential Listeria Contamination
Old Europe Cheese is recalling LA BONNE VIE and Reny Picot brand Cranberry Baked Brie cheese due to potential Listeria monocytogenes contamination.
Product
LA BONNE VIE 11 oz Cranberry Baked Brie UPC 820581678821; Reny Picot 11 oz Cranberry Baked Brie UPC 033421051115
Category
Food
Distribution
25 states
SevereCPSC·23030·2022-11-03
Power Plus Tora Portable Power Charging Stations Recalled for Fire and Explosion Hazard
Power Plus is recalling about 115 Tora portable power charging stations because the lithium-ion battery can catch fire while charging. Two fires have been reported with no injuries.
Product
Power Plus Tora Portable Power Charging Stations
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23034·2022-11-03
BLACK+DECKER Garment Steamers Recalled for Burn Hazard from Hot Water
Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.
Product
BLACK+DECKER Model HGS011 Easy Garment Steamers
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0019-2023·2022-11-02
Atenolol 25mg bottles mislabeled; contain Clopidogrel 75mg tablets
Golden State Medical Supply Inc. is recalling 2,584 bottles of Atenolol 25mg tablets nationwide. Bottles labeled as Atenolol 25mg actually contain Clopidogrel 75mg tablets—a different medication.
Product
ATENOLOL — ATENOLOL (ATENOLOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0023-2023·2022-11-02
Sodium Bicarbonate Injection Recalled for Defective Vials and Glass Breakage
Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.
Product
8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0140-2023·2022-11-02
Earth Grown Vegan Falafel Recalled for Possible E. coli Contamination
Earth Grown Vegan Traditional Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The FDA Class I recall affects approximately 190,860 units distributed across multiple U.S. states.
Product
Earth Grown Vegan Traditional Falafel NET WT 12 OZ (340g), 12 pieces UPC:4 0991002 24337
Category
Food
Distribution
18 states
SevereFDA (Food)·F-0141-2023·2022-11-02
Earth Grown Vegan Falafel Recalled for E. Coli Contamination
Earth Grown Vegan Garlic & Herb Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The recall affects over 190,000 units distributed across multiple US states.
Product
Earth Grown Vegan Garlic & Herb Falafel NET WT 12 OZ (340g), 12 pieces UPC:4 0991002 24344
Category
Food
Distribution
18 states
SevereFDA (Drugs)·D-0022-2023·2022-11-02
Sodium Bicarbonate Injection Recalled for Defective Vials with Glass Breakage Risk
Exela Pharma Sciences is recalling 2,123,040 vials of Sodium Bicarbonate 8.4% Injection due to container defects causing vial breakage and glass release when pressurized during product preparation.
Product
SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0117-2023·2022-11-02
Caribou Coffee Snack Fruit and Cheese Plate Recalled for Listeria Risk
Cut Fruit Express is recalling Caribou Coffee Snack Fruit and Cheese Plates due to potential Listeria in the Brie cheese. Affected units were distributed in Minnesota with Use By dates from September 30 to October 9, 2022.
Product
Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Net Wt 6.2 oz. (176g) 3 cheeses, red grapes, apples, rosemary crackers. Keep Refrigerated. Manufactured By: Cut Fruit Express, Inver Grove Heights, MN
Category
Food
Distribution
1 state
SevereNHTSA·22V817000·2022-11-01
Brake modulator corrosion recall on Freightliner and Western Star commercial trucks
Daimler Trucks North America is recalling certain Freightliner Cascadia and Western Star models due to corrosion in front brake modulator valves. The defect may cause brakes to pull to one side during automated braking, increasing crash risk.
Product
FREIGHTLINER — 2017 FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V816000·2022-10-31
2021 Hyundai Santa Fe Hybrid seat belt pretensioners may explode in crash
Hyundai is recalling 2021-2023 Santa Fe Hybrid and 2022-2023 Santa Fe Plug-In Hybrid vehicles, plus 2023 Genesis G80 Electric vehicles, because seat belt pretensioners may explode in a crash and project metal fragments. Dealers will secure the pretensioners with a cap at no cost.
Product
HYUNDAI — 2021 HYUNDAI SANTA FE HYBRID
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·23027·2022-10-27
Goalsetter Wall-Mounted Basketball Goals Recall Due to Detachment Hazard
Goalsetter is recalling about 18,000 wall-mounted basketball goals because they can detach from walls and fall. One fatality and multiple injuries have been reported.
Product
Goalsetter wall-mounted basketball goals
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23026·2022-10-27
Horizon T101-05 Treadmills Recalled for Unexpected Speed and Stop Hazard
Horizon T101-05 folding treadmills can unexpectedly accelerate, change speed, or stop without user input, posing a fall hazard. About 192,000 units sold in the U.S. are affected; 71 injuries including broken bones have been reported.
Product
Horizon T101-05 Treadmills
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23705·2022-10-27
LG Energy Solution RESU 10H Batteries Recalled for Fire Hazard
LG Energy Solution is recalling about 11,500 RESU 10H lithium-ion residential energy storage batteries because they can overheat and pose a fire risk with harmful smoke emissions. One incident of smoking and fire with property damage has been reported.
Product
LG Energy Solution "RESU 10H" Lithium-Ion Residential Energy Storage System Batteries
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0074-2023·2022-10-26
Medical Gas Filter Devices Recalled Due to Splitting and Detachment Risk
Teleflex is recalling Iso-Gard Filter S microbial medical gas filters that may split or detach during use. The recall affects 164 units distributed nationwide.
Product
Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0080-2023·2022-10-26
Fenugreek dietary supplement recalled for potential Salmonella contamination
Best Nutritionals LLC is recalling Best Naturals Fenugreek 610mg capsules due to potential Salmonella contamination. The product was distributed online via internet sellers and FBA.
Product
White plastic bottle with green, gold, and blue labeling containing 360, 610mg hard gelatin capsules of Fenugreek seed powder, labeled in part, "Best Naturals Fenugreek Premium Herbal 610mg 3rd Party Lab Tested 360 CAPSULES DIETARY SUPPLEMENT", best by 10/24, lot 102120
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-0073-2023·2022-10-26
Iso-Gard Filter S Medical Gas Filter Recall Due to Splitting or Detachment
TELEFLEX LLC is recalling Iso-Gard Filter S microbial medical gas filters due to incidents where the device may split or detach during use. The FDA classified this as a Class I recall.
Product
Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medical gas filter, single-use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0076-2023·2022-10-26
Medical gas filter recalled due to splitting and detachment risk
TELEFLEX LLC is recalling Iso-Gard Filter S medical gas filters due to incidents of device splitting or detaching during use. The affected filters may compromise patient safety.
Product
Iso-Gard Filter S with Expandi-Flex/Elbow: a) REF 19012, OUS only, b) REF 19012T with Tethered Cap, OUS only; Microbial medical gas filter, single-use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0072-2023·2022-10-26
Iso-Gard Filter S Recalled for Device Splitting or Detachment During Use
Teleflex is recalling Iso-Gard Filter S microbial filters (60,500 units) due to incidents of device splitting or detaching during use. The filters protect patients and equipment from bacterial and viral contamination in breathing systems.
Product
Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral filters for use in breathing system for the protection of patient and equipment.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0038-2023·2022-10-26
Dark Chocolate Almonds recalled for undeclared milk allergen
Dark Chocolate Almonds sold at Safeway, Albertsons, and Roths Fresh Market contain undeclared milk allergen. The FDA Class I recall affects 1,701 cases distributed in Oregon and Washington.
Product
Dark Chocolate Almonds distributed to Safeway/Albertsons is packaged in a clear clamshell container with a top label that displays PRODUCE Dark Chocolate Almonds , net weight of 9.5 oz., UPC 0 19061 19371 2. Distributed by Rivertrail Foods with an address of 4660 Ridge Dr. NE. S
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-0075-2023·2022-10-26
Iso-Gard Filter S Medical Gas Filters Recalled Due to Device Splitting Risk
TELEFLEX is recalling 355 units of Iso-Gard Filter S medical gas filters nationwide due to incidents of device splitting or detaching during use. The FDA classified this as a Class I recall.
Product
Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter, single-use,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0077-2023·2022-10-26
Teleflex Catheter Mount and Filter May Split or Detach During Use
Catheter mounts with filters (REF 191667-000100) used to connect endotracheal tubes or masks to breathing circuits may split or detach during patient use. Teleflex is recalling affected units distributed nationwide.
Product
Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection (Endotracheal tube and mask)
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V799000·2022-10-22
CAN-AM Ryker Motorcycles Recalled for Loose Harnesses Causing Engine Stall
CAN-AM is recalling 2019-2023 Ryker motorcycles because electrical harnesses in the front fenders may loosen and rub on the tire, causing a short circuit that can stall the engine while driving.
Product
CAN-AM — 2021 CAN-AM RYKER
Category
Vehicle
Distribution
Distributed nationwide

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5526–5550 of 7463