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

5751–5775 of 7476

SevereFDA (Food)·F-1602-2022·2022-09-07
Glucerna original Vanilla Shake recalled for bacterial contamination
Lyons Magnus is recalling Glucerna original Vanilla Shake due to findings of Cronobacter sakazakii and potential Clostridium botulinum. Over 53 million units were distributed nationwide.
Product
Glucerna original Homemade Vanilla Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68563 2. Sold in 24 count case, Case UPC 0070074685625. Shake Well. Serve cold. Refrigerate after opening. Manufactured for: Abbott Nutrition, Abbott Labor
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1628-2022·2022-09-07
MRE Salted Caramel Protein Shake Recalled for Cronobacter and Botulinum Risk
Lyons Magnus recalls MRE Salted Caramel Protein Shake nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. Consumers should not consume affected products.
Product
MRE Salted Caramel Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57392 3. 4-count case UPC 810044573930. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1631-2022·2022-09-07
Sysco Imperial Dairy Drink Recalled for Cronobacter and Botulism
Lyons Magnus recalled Sysco Imperial Thickened Dairy Drink nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. The FDA Class I recall affects over 53 million units distributed in 8 oz and 32 oz containers.
Product
Sysco Imperial Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Made with Grade A 2% Fat Milk, Vitamins A & D. Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 74865-94550 9. Reorder # 0429357. 24 count case UPC
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1629-2022·2022-09-07
MRE Vanilla Protein Shake Recalled for Potential Bacterial Contamination
Lyons Magnus is recalling MRE Vanilla Protein Shake nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria.
Product
MRE Vanilla Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57390 9. 4-count case UPC 810044573954. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1670-2022·2022-09-07
Kate Farms Nutritional Formula Recalled for Cronobacter and Botulism Risk
Kate Farms Standard 1.4 Cal/mL nutrition formula in 325 mL bottles is recalled nationwide due to potential Cronobacter sakazakii and Clostridium botulinum. Affected lot code 8031 has best-by date November 4, 2022.
Product
kate farms Standard 1.4 Cal/mL, Plain, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 11112-03001 0. 12 count case UPC 00811112030027. Shake Well. A ready-to-use oral and tube feeding formula. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 9370
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1666-2022·2022-09-07
Kate Farms Nutrition Formula Recalled for Cronobacter and Botulinum Risk
Kate Farms Standard nutrition formula in 325 mL bottles is being recalled due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Approximately 53,818,025 units distributed nationwide.
Product
kate farms Standard 1.0 Cal/mL, Vanilla, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 51823-00663 8. 12 count case UPC 00851823006683. Shake Well. A ready-to-use oral and tube feeding formula with intact organic pea protein. Made for Kate Farms, Inc., 101 Innovat
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·22V663000·2022-09-01
Jayco and Entegra motorhomes recalled for suspension torsion bar defect
Entegra and Jayco motorhomes may have incorrectly installed torsion bar shims causing potential suspension failure. Dealers will replace the defective component free of charge.
Product
ENTEGRA — 2021 ENTEGRA QWEST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V662000·2022-09-01
Honda CRF1100 Africa Twin Motorcycles Recalled for Engine Control Software Bug
Honda is recalling 2020-2021 CRF1100 Africa Twin motorcycles due to an ECU software error that may cause engine stall or loss of drive power. Owners can get a free software update from dealers.
Product
HONDA — 2021 HONDA CRF1100 AFRICA TWIN
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·22215·2022-09-01
UPPAbaby RIDGE Jogging Strollers Recalled for Fingertip Amputation Hazard
UPPAbaby is recalling about 14,400 All-Terrain RIDGE jogging strollers because openings in the rear disc brakes can catch and amputate a child's fingertip. One injury has been reported.
Product
UPPAbaby All-Terrain RIDGE Jogging Strollers
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1522-2022·2022-08-31
INTERA 3000 implantable pump recalled for higher-than-expected flow rate
The FDA is recalling INTERA 3000 implantable hepatic infusion pumps due to a malfunction causing higher-than-expected medication flow rates. Patients should contact their healthcare provider.
Product
INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1560-2022·2022-08-31
Getinge Servo ventilator systems recalled for loss of ventilation
Getinge Servo ventilators may fail to deliver ventilation and stop functioning, potentially causing oxygen deprivation and serious harm to critical care patients.
Product
Maquet Critical Care AB/Getinge Servo-u Ventilator System, Part Number 6694800 Servo-n Ventilator System, Part Number 6688600 Servo-u MR ventilator: Part Number 6888800 Servo-air: Part Number 6882000
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1576-2022·2022-08-31
Tovala Salmon Meal Recalled Due to Undeclared Peanut Allergen
Tovala is recalling its Gochujang-Glazed Salmon Bowl meal (No. 18-A) because it contains an undeclared peanut allergen. The affected products were distributed nationwide to consumers.
Product
Tovala Gochujang-Glazed Salmon Bowl meal No.18-A
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1561-2022·2022-08-31
Diaphragm pacing system external pulse generator recalled for circuit board defect
Synapse Biomedical is recalling the NeuRx Diaphragm Pacing System External Pulse Generator due to a circuit board defect causing performance degradation, potentially leading to cardiac complications, breathing failure, or device shutdown.
Product
NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021.
Category
Medical Device
Distribution
12 states
SevereFDA (Food)·F-1577-2022·2022-08-31
Tovala gochujang pork bowl meals recalled for undeclared peanut allergen
Tovala is recalling approximately 3,340 Gochujang-Glazed Pork Chop Bowl meals distributed nationwide because they contain undeclared peanuts, which pose an allergy risk to consumers with peanut allergies.
Product
Tovala Gochujang-Glazed Pork Chop Bowl meal No.9-A
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1525-2022·2022-08-31
Intensive care ventilator status board may loosen, causing water damage and malfunction
Hamilton's HAMILTON-C6 intensive care ventilator status indicator board may become loose, allowing water or disinfectants to enter the device and cause technical faults that could force the ventilator into unsafe modes where patients breathe unassisted room air.
Product
HAMILTON-C6 Intensive Care Ventilator, REF: 160021
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·22210·2022-08-25
Stand-up Paddleboard Paddles Recalled for Puncture and Laceration Risk
Agit Global stand-up paddleboard paddles can suddenly break mid-shaft during use, exposing sharp edges. About 124,000 units sold nationwide from 2015–2020 pose a risk of serious puncture or laceration injuries.
Product
Paddles sold with stand-up paddleboards
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·22V639000·2022-08-25
2022 Jeep Gladiator Transmission Park Mechanism Defect Recall
Chrysler is recalling certain 2022 Jeep Gladiator vehicles due to a defective transmission park pawl that may not properly engage, potentially causing vehicle rollaway.
Product
JEEP — 2022 JEEP GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1342-2022·2022-08-24
Hand sanitizer recalled for methanol contamination and insufficient ethanol
Medek LLC is recalling M Hand Sanitizer due to FDA analysis finding methanol contamination and ethanol levels below label claims. Approximately 256 bottles distributed in Texas.
Product
M Hand Sanitizer Ethyl Alcohol Antiseptic 80%v/v, Topical Solution 128 oz/3,785 mL, Made in Mexico by: Grupo Plast-Y-Kosas S.A. de C.V. Puebla 105 Col. Rodriguez Reynosa, Tam, Mexico C.P. 88630, NDC Code: 77797-001-01, Distributed by: Medek, LLC 315 E. Business Hwy 83 Alamo, TX
Category
Drug
Distribution
0 states
CriticalFDA (Food)·F-1596-2022·2022-08-24
Kingdom Creamery 8.5% Gelato Mix Products Recalled for Potential Listeria Contamination
Kingdom Creamery of Vermont is recalling 8.5% Gelato Mix due to potential Listeria monocytogenes contamination. The recall involves 1,623 cases distributed in Vermont, Maine, and Massachusetts.
Product
SOCO 8.5% Gelato Mix; 8.5% Gelato Mix; both labels list Kingdom Creamery of Vermont
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1593-2022·2022-08-24
Kingdom Creamery Vermont 14% Base Mix Recalled for Listeria Contamination
Kingdom Creamery of Vermont's 14% Base Mix is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
Product
14% Base Mix; Kingdom Creamery of Vermont
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1595-2022·2022-08-24
Lake Champlain Chocolates 14% base mix recalled for Listeria monocytogenes
Kingdom Creamery of Vermont LLC is recalling Lake Champlain Chocolates 14% base mix due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
Product
Lake Champlain Chocolates 14% base mix
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1591-2022·2022-08-24
Kingdom Creamery Vermont Chocolate Soft Serve Mix Recalled for Listeria
Kingdom Creamery of Vermont 10% Chocolate Soft Serve Mix is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.
Product
Kingdom Creamery of Vermont 10% Chocolate Soft Serve Mix
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1586-2022·2022-08-24
FDA Recalls Kingdom Creamery Vanilla Soft Serve Mix for Listeria Risk
Kingdom Creamery of Vermont is recalling 5% Vanilla Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.
Product
Kingdom Creamery of Vermont 5% Vanilla Soft Serve Mix
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1589-2022·2022-08-24
Kingdom Creamery of Vermont Maple Soft Serve Mix Recalled for Listeria
Kingdom Creamery of Vermont's 10% Maple Soft Serve Mix is being recalled due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.
Product
Kingdom Creamery of Vermont 10% Maple Soft Serve Mix
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1592-2022·2022-08-24
Vermont creamery recalls ice cream base mix due to Listeria contamination
Kingdom Creamery of Vermont is recalling 14% Base Mix and Archie Case Mix ice cream base products due to Listeria monocytogenes contamination. A Class I FDA recall affects 1,623 cases distributed to Vermont, Maine, and Massachusetts.
Product
14% Base Mix Case:14% Archie Case Mix
Category
Food
Distribution
3 states

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