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

13126–13150 of 27722

HighFDA (Drugs)·D-0437-2024·2024-04-17
FDA Recalls Rifampin Capsules 300mg Nationwide for Subpotency
Lupin Pharmaceuticals recalls Rifampin Capsules USP 300mg nationwide due to subpotency—the drug contains less active ingredient than labeled. Affected lot: A201064, expiring March 2024. 26,352 bottles involved.
Product
Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India, NDC 6818-0659-06
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2024·2024-04-17
Feeding tube kit recalled due to blocked connector preventing guidewire advancement
Boston Scientific's EndoVive 20Fr PEG kit may have a blocked connector preventing proper guidewire advancement during placement, potentially requiring emergency intervention.
Product
EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00566471
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2024·2024-04-17
Femoral Resurfacing Cup Components Marketed Without Required FDA Clearance
Synovo Production recalled 496 femoral resurfacing cup components that were marketed without FDA clearance. These hip implant components were distributed in the United States.
Product
Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V ELI, TiN CERAMIC W/ PLASMA SPRAY, STERILEEO, Reference Numbers: 01-03-0042 01-03-0044 01-03-0045 01-03-0047 01-03-0049 01-03-0051 01-03-0052
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1122-2024·2024-04-17
Ground cinnamon bulk product recalled due to elevated lead levels
Tasty-Sawa ground cinnamon in 55.11-pound bags distributed in Florida, Georgia, North Carolina, Trinidad and Tobago, and Guyana is being recalled due to elevated lead levels. Consumers should stop using this product immediately.
Product
Tasty-Sawa Cinnamon Ground, Net Wt. 55.11 lbs, paper bag (bulk), Country of Origin Vietnam
Category
Food
Distribution
3 states
SevereCPSC·24743·2024-04-11
Matrix T1 and T3 Commercial Treadmills Fire Hazard Expansion Recall
Johnson Health Tech North America is expanding its recall of Matrix T1 and T3 Series commercial treadmills due to a fire hazard from loose power cords. About 9,700 additional units are affected.
Product
Matrix T1 and T3 Series Commercial Treadmills
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24199·2024-04-11
Zipline Kits Recalled Due to Cable-Breaking Fall Hazard
Jugader Zipline Kits sold on Amazon.com from March 2020 through June 2023 are recalled because the stainless-steel cable can break, causing falls. The manufacturer has received 20 reports of cable breakage resulting in nine injuries.
Product
Zipline Kits
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V771000·2024-04-11
2023 Jayco Alante and Related Motorhomes Recalled for Instrument Panel Corrosion
Jayco is recalling 2023-2024 motorhomes where corrosion in an electrical connector can disable the instrument panel, preventing display of the speedometer and warning lights.
Product
JAYCO — 2023 JAYCO ALANTE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24190·2024-04-11
Yoto Mini Speakers Recalled for Burn and Fire Hazards
Yoto Mini portable speakers for children ages 3–12 are being recalled because the lithium-ion battery can overheat and catch fire. Consumers should stop using them immediately and contact Yoto for a free replacement charging cable.
Product
Yoto Mini speakers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V878000·2024-04-11
2023 Kia Sportage Curtain Airbags May Deploy Improperly Due to Installation Twist
Kia is recalling 76,918 model year 2023 Sportage vehicles with potentially twisted side curtain airbags that may deploy improperly, increasing the risk of injury.
Product
KIA — 2023 KIA SPORTAGE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24192·2024-04-11
BRS Liquid Fuel Bottles Recalled for Non-Child-Resistant Closure Risk
About 1,600 BRS portable liquid fuel bottles with non-child-resistant closures have been recalled due to risk of burn and poisoning to children. The closure does not meet requirements of the Children's Gasoline Burn Prevention Act.
Product
BRS Liquid Fuel Bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24193·2024-04-11
Red Land Cotton Recalls Quilts and Shams Due to Laceration Hazard
Red Land Cotton is recalling approximately 17,400 quilts and quilted shams sold on Amazon.com because pieces of broken needles inside the products pose a laceration hazard. The company has received three reports of consumers being jabbed by sharp metal needles.
Product
Red Land Cotton "Quilts" and "Quilted Shams"
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V770000·2024-04-11
2024 BMW X3 and Related Models: Loose Steering Gear Recall
BMW is recalling certain 2024 BMW X3 and related models due to steering gear that may not have been properly tightened, which can loosen and cause loss of vehicle control. Dealers will replace the steering gear free of charge.
Product
BMW — 2024 BMW X3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V829000·2024-04-11
2025 BMW X1 B-Pillar Structure Defect May Reduce Crash Protection
Certain 2025 BMW X1 vehicles have B-Pillar reinforcement plates with insufficient structural strength. This defect may reduce crash protection and increase injury risk.
Product
BMW — 2025 BMW X1
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24196·2024-04-11
Intimidator and Mahindra Utility Vehicles Recalled for Brake Line Failure Hazard
About 19,264 Intimidator and Mahindra UTVs are recalled because the universal joint can fail and sever the brake line, posing a crash hazard. No injuries have been reported. Owners should immediately stop using the vehicles and contact a dealer for free repair.
Product
Intimidator and Mahindra branded utility vehicles (UTVs)
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1356-2024·2024-04-10
iQ 2 Nasal Vented Mask Recalled for Magnet Safety Warnings
SleepNet Corporation is recalling the iQ 2 Nasal Vented Mask due to magnets requiring updated contraindication and warning language. Approximately 2,477 units distributed worldwide are affected.
Product
iQ 2 Nasal Vented Mask
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1357-2024·2024-04-10
Phantom 2 Nasal Vented Mask recalled due to magnetic device interference risk
SleepNet is recalling the Phantom 2 Nasal Vented Mask to update contraindications and warning information related to magnets in the device. The recall affects 2,417 units distributed worldwide.
Product
Phantom 2 Nasal Vented Mask
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1116-2024·2024-04-10
Dark Chocolate Cherry Granola Recalled Due to Undeclared Almond Allergen
Kick Ash Products is recalling Dark Chocolate Cherry Granola because it contains undeclared almond, a common allergen. Affected products may be unsafe for individuals with almond allergies.
Product
Kick Ash Products, Door County Love Dark Chocolate Cherry Granola, 1lb, laminated resealable bag
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1355-2024·2024-04-10
Mojo 2 CPAP Masks Recalled Worldwide for Magnet Safety Contraindication Update
SleepNet Corporation is recalling Mojo 2 Full Face CPAP masks (1,268 units worldwide) to update contraindications and warning language due to magnets in the masks. The FDA classified this as a Class I recall.
Product
Mojo 2 Full Face AAV Non Vented Mask, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1353-2024·2024-04-10
Mojo 2 Full Face Vented Mask Recalled: Magnet Contraindications Updated
SleepNet Corporation is recalling 2,787 units of the Mojo 2 Full Face Vented Mask due to updates needed for contraindications and warning language regarding magnets in the device. Worldwide distribution.
Product
Mojo 2 Full Face Vented Mask, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1354-2024·2024-04-10
Mojo 2 Full Face Non Vented Mask Recalled for Magnet Safety Concerns
SleepNet Corporation is recalling Mojo 2 Full Face Non Vented Masks due to magnets in the device and updated contraindications and warnings. The recall affects 2,107 units distributed worldwide.
Product
Mojo 2 Full Face Non Vented Mask, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1352-2024·2024-04-10
Mojo Non Vented Full Face Mask warning updated for magnet hazard
SleepNet is updating safety warnings and contraindications for its Mojo Non Vented Full Face Mask due to magnet content. All 11,874 affected units are subject to this warning update.
Product
Mojo Non Vented Full Face Mask with Headgear, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1114-2024·2024-04-10
Soy bean sprouts recalled for Listeria monocytogenes contamination
Samsung Bean Sprout is recalling 500 bags of Sam Sung Soy Bean Sprouts with a sell-by date of December 21, 2023, distributed in Virginia, due to potential Listeria monocytogenes contamination.
Product
Soy Bean Sprouts in a package labeled in part: Sam Sung Soy Bean Sprouts, Net Wt. 1LB have a Sell By date of December 21, 2023.
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1351-2024·2024-04-10
Mojo Full Face CPAP Mask Recall: Magnet Safety Update
SleepNet Corporation is recalling 23,042 Mojo Full Face CPAP masks worldwide because the masks contain magnets that require updated contraindications and warning language.
Product
Mojo Full Face with Headgear, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1445-2024·2024-04-10
Suture Removal and Staple Remover Kits Recalled for Weak Seal
Medline Industries is recalling suture removal trays and staple remover kits due to weak seals that may compromise product sterility. Approximately 23,290 units were distributed in the US, Panama, and Canada.
Product
Centurion manual surgical kits labeled as: a) SUTURE REMOVAL TRAY, Product Code TRI55405; b) SUTURE REMOVAL SET, Product Code 60265 MEDLINE manual surgical kits labeled as: a) SUTURE REMOVAL TRAY, Product Code 60280; b) SUTURE REMOVAL TRAY, Product Code 86125; c) SUT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1407-2024·2024-04-10
Exactech Equinoxe Shoulder Glenoid Components Recalled for Defective Packaging
Exactech is recalling 985 shoulder implant components due to nonconforming packaging that lacks a required oxygen barrier layer. The vacuum bags do not meet packaging specifications.
Product
Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTED, 8o, RIGHT, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-02-32, b) 41, 44, 47, 50 head, Medium, Item Number 314-02-33, c) 44, 47, 50, 53 head, Large, Item Number 314-02-34, d) 44, 47, 50, 53 he
Category
Medical Device
Distribution
Distributed nationwide

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13126–13150 of 27722