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

11851–11875 of 27719

HighFDA (Devices)·Z-2330-2024·2024-07-17
Presource Neurological Surgical Kits Recalled for Syringe Design Defect
Cardinal Health is recalling Presource neurological surgical kits containing defectively designed syringes that may cause inaccurate dosing or device leakage. The recall affects 13,487 kits distributed nationwide.
Product
Presource kits and trays, labeled as: 1) Neurological Tray, Catalog Number SAN29NICCA; 2) Neurological Tray, Catalog Number SAN29NRCC1; 3) Neurological Tray, Catalog Number SAN29NRCC2; 4) Neurological Tray, Catalog Number SAN29NRCC3; 5) Neurological Tray, Catalog Number SAN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2310-2024·2024-07-17
Hand Procedure Kit Recalled for Excess Ethylene Oxide Residuals
American Contract Systems recalls HAND PACK-Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residuals on the cast padding component, exceeding safe permanent-contact exposure limits.
Product
HAND PACK-Procedure Kit Catalog Number: WEHD16B
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V862000·2024-07-12
2022-2023 Tesla Model S and X Door Latch Safety Defect Recall
Certain 2022-2023 Tesla Model S and X vehicles may have cabin doors that unlock during a crash due to a door latch defect. Tesla is providing a free over-the-air software update to fix the issue.
Product
TESLA — 2022 TESLA MODEL S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V860000·2024-07-12
Airstream Basecamp Travel Trailers Recalled for Failing Spare Tire Bracket
The spare tire carrier bracket on certain 2012-2023 Airstream Basecamp travel trailers may experience metal fatigue and break, causing the spare tire to detach and become a road hazard. Airstream is providing free replacement and reinforcement of the bracket.
Product
AIRSTREAM — 2023 AIRSTREAM BASECAMP
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·24302·2024-07-11
Best Lighting Products LED High Bay Light Fixtures Recalled for Fire Hazard
Best Lighting Products is recalling approximately 710,600 LED High Bay Light Fixtures because plastic pins securing the LED board can degrade, allowing the energized board to come loose and pose a fire hazard. Three fires have been reported.
Product
LED High Bay Light Fixtures
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V839000·2024-07-11
2022-2023 Chevrolet Express and GMC Savana transmission software defect
GM is recalling 2022-2023 Chevrolet Express and GMC Savana vehicles for a transmission software defect that may cause rear wheel lockup and unintended vehicle movement. Dealers will update the software free of charge.
Product
GMC — 2023 GMC SAVANA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24303·2024-07-11
TonGass Pool Drain Covers Recalled for Entrapment Hazard
TonGass 8-inch round pool drain covers do not meet Virginia Graeme Baker Pool and Spa Safety Act standards and pose an entrapment hazard to swimmers and bathers. About 1,650 units sold on Amazon from September 2023 through June 2024 are affected.
Product
TonGass pool drain covers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24299·2024-07-11
Claire's and Icing Stores Halloween Witch Hats Burn Hazard Recall
Claire's and Icing stores are recalling about 5,700 Halloween witch hats sold nationwide from July through December 2023. The hats violate federal flammability requirements and pose a risk of burn injuries.
Product
Halloween Witch Hats
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24296·2024-07-11
Children's Pajama Sets Recalled for Flammability Hazard
About 45,300 children's two-piece pajama sets sold on Temu.com violate federal flammability standards for sleepwear, posing a burn risk to children. Consumers should immediately stop using the garments and contact Fashion Online for a refund.
Product
Children's Long-Sleeve/Pants Two-Piece Pajama Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24298·2024-07-11
Atomi Smart Heaters recalled for fire and burn hazards
Atomi Smart Heaters can turn on without user input, creating fire and burn risks. About 99,400 units sold nationwide are affected; consumers should stop use immediately and follow refund instructions.
Product
Atomi Smart Heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V843000·2024-07-11
2024 Hyundai Santa Fe sunshade switch defect increases injury risk
Hyundai is recalling 34,964 units of the 2024 Santa Fe and Santa Fe Hybrid with faulty switch knobs that may not retract, creating an injury risk.
Product
HYUNDAI — 2024 HYUNDAI SANTA FE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24301·2024-07-11
Children's Pajama Sets Recalled for Burn Hazard and Flammability Violation
JUVENNO KIDS is recalling about 18,620 children's button-up pajama sets sold on Temu.com because they violate federal flammability standards for sleepwear and pose a burn injury risk to children. No injuries have been reported.
Product
Children's Button-up Short-Sleeve/Shorts Two-Piece Pajama Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24300·2024-07-11
Children's Lace Nightgowns Recalled for Burn Hazard
Lovely Angel children's lace nightgowns sold on Temu.com violate federal flammability standards for sleepwear, posing a burn injury risk to children. About 4,360 units were sold between June 2023 and May 2024.
Product
Lovely Angel Children's Lace Nightgowns
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-1431-2024·2024-07-10
Walmart Great Value Organic Black Chia Seeds Recalled for Salmonella Contamination
Walmart Great Value Organic Black Chia Seeds (32 oz) are being recalled due to potential Salmonella contamination. The product was distributed to multiple states.
Product
Walmart Great Value Organic Black Chia Seeds 32 oz.
Category
Food
Distribution
12 states
SevereFDA (Devices)·Z-2248-2024·2024-07-10
Megadyne MEGA 2000 Patient Return Electrode recalled for burn risk
Megadyne is recalling the MEGA 2000 Patient Return Electrode due to identified potential risk of patient burns. Use is now restricted to patients aged 12 or older.
Product
Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patient Return Electrode Model/Catalog Number: 0800 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega 2000, Adult, For Patients Weighing over 25lbs. (
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0586-2024·2024-07-10
Horny Goat Weed Capsules Recalled for Undeclared Sildenafil
To the Moon Capsules are being recalled nationwide because they contain undeclared sildenafil, a prescription pharmaceutical. The product was marketed without FDA approval.
Product
To the Moon Capsules, Horny Goat Weed, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0585-2024·2024-07-10
RAM IT Horny Goat Weed Dietary Supplement Recalled for Undeclared Sildenafil
Integrity Products recalls RAM IT Horny Goat Weed dietary supplement capsules nationwide because they contain undeclared sildenafil, a prescription drug not listed on the label.
Product
RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2250-2024·2024-07-10
Reusable Patient Return Electrode Recalled Due to Burn Risk
MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrodes are recalled due to an identified risk of patient burns. Use should be restricted to patients aged 12 or older.
Product
Brand Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Model/Catalog Number: 0835 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Dual Cord, Adu
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2249-2024·2024-07-10
MEGADYNE MEGA SOFT Reusable Patient Return Electrode Recalled for Burn Risk
Megadyne Medical recalls MEGA SOFT reusable patient return electrodes (Model 0830) due to identified burn risk. Use is restricted to patients aged 12 and older.
Product
Brand Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Model/Catalog Number: 0830 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Single Cord, Adult, For
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1432-2024·2024-07-10
Thyroid Supplement Recalled for Potential Salmonella Contamination
Penn Herb Company is recalling Nature's Wonderland brand Thyroid Formula due to potential Salmonella contamination. Fifty-one bottles were distributed across nine states.
Product
Nature's Wonderland brand Thyroid Formula 60 Veg Capsules UPC: 715486893205. Packaged in White PET 150cc bottle with security closure
Category
Food
Distribution
9 states
SevereNHTSA·22V816000·2024-07-10
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
HighFDA (Devices)·Z-2224-2024·2024-07-10
Medline surgical convenience kits recalled for weak seal defects
Medline Industries is recalling 12,588 sterile surgical convenience kits due to weak seals on Pure Pouch components that may breach sterility. Products were distributed nationwide across 23 states.
Product
Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure, Pack #00-RDF0360, containing a Pure Pouch with component Medline Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile. b. Medline Angiography Pack, Pack #DYNJ26488W, containing a Pure Pouch with compo
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2265-2024·2024-07-10
Abbott Liberta RC Pulse Generator Unexpectedly Shuts Down Periodically
Abbott Liberta RC implantable pulse generators used for deep brain stimulation may unexpectedly turn off approximately every 50 days after activation, resulting in loss of therapy. Approximately 302 units have been recalled nationwide.
Product
Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2237-2024·2024-07-10
Beckman Coulter DxI 9000 Analyzer Tubing Malfunction Causes Test Errors
Beckman Coulter DxI 9000 immunoassay analyzers may produce false or delayed test results due to pneumatic tubing disconnection during operation. Nine instruments are affected across the US and Europe.
Product
Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete photometric chemistry analyzer for clinical use. It is an in-vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human bod
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2247-2024·2024-07-10
X-ray cart positioning arm bolt may loosen and fall onto patient
A bolt securing the positioning arm on First Source iQ Flex M X-ray carts may come loose and fall onto patients. The recall involves 137 units distributed across the US, Korea, and Serbia.
Product
First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer.
Category
Medical Device
Distribution
Distributed nationwide

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11851–11875 of 27719