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

11051–11075 of 27647

HighFDA (Devices)·Z-2623-2024·2024-09-04
Medline procedure packs with syringes recalled due to leaks and breakage
Medline is recalling procedure packs containing Shenli syringes due to leaks, breakage, and quality issues that may pose risks to patient health. Over 1.6 million units have been distributed worldwide.
Product
Medline procedure packs containing Shenli syringes, labeled as follows: 1) LOCAL PACK, pack number DYNJ34129C, 2) FTMC LOCAL PACK-LF, pack number DYNJ54607A, 3) LOCAL PACK, pack number DYNJ61839B
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2838-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled
Beaver Visitec International recalls BVI CustomEyes Procedure Packs containing Sol-M brand syringes due to manufacturer's voluntary recall. 130 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001020;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2723-2024·2024-09-04
Stryker iBur 4.0mm surgical bur recall: excessive heat risk during bone surgery
Stryker iBur 4.0mm precision surgical burs may overheat where the shank meets the distal bushing. Excessive heat could cause minor tissue damage or thermal injury requiring medical intervention.
Product
Stryker iBur 4.0mm Precision Round, Distal Bend- intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; an
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2797-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled for Sol-M Syringe Components
Beaver Visitec International voluntarily recalls BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The recall affects 351 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000126;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2886-2024·2024-09-04
BVI CustomEyes Procedure Packs containing Sol-M Syringes Recalled Nationwide
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M-manufactured syringes. The recall affects 138 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001579;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2759-2024·2024-09-04
Medline Procedural Kits Recalled for Syringe Quality Defects
Medline is recalling NEURO TRAY procedural kits (Pack DYNJ55909B, Lot 23IBB122) due to plastic syringe defects including leaks and breakage that may pose a risk to patient health.
Product
Medline procedural kits labeled as: NEURO TRAY, Pack Number DYNJ55909B
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1753-2024·2024-09-04
Ground cinnamon recalled due to elevated lead levels
Colonna Brothers Inc. is recalling Supreme Tradition and Marcum brand ground cinnamon distributed nationwide due to elevated lead levels.
Product
Ground cinnamon. Supreme Tradition brand ground cinnamon packaged in 2.25 oz clear plastics jars with black lids. UPC: 639277656377 Marcum brand ground cinnamon packaged in 1.5 oz clear plastic jars with black lids. UPC:051933364035
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2747-2024·2024-09-04
Medline Procedural Kits Recalled Due to Defective Plastic Syringes
Medline is recalling multiple procedural kits containing plastic syringes that may leak, break, or have quality defects. These defects may pose a risk to patient health during surgical procedures.
Product
Medline procedural kits labeled as: 1) TYMPANOPLASTY , Pack Number CDS980203S; 2) MAJOR EAR , Pack Number CDS982016T; 3) MAJOR EAR PACK, Pack Number CMPJ01846O; 4) EAR PACK, Pack Number CMPJ05884J; 5) MZ EAR PACK , Pack Number CMPJ09860D; 6) KIT MAJOR EAR CHRG, Pack
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2756-2024·2024-09-04
Medline Procedural Kits Recalled Due to Defective Plastic Syringes
Medline Industries is recalling multiple procedural kits containing defective plastic syringes that may leak or break. The affected kits were distributed worldwide.
Product
Medline procedural kits labeled as: 1) CIRCUMCISION TRAY, Pack Number CIT6715; 2) NICU CIRCUMCISION TRAY W/OUT CLAMP, Pack Number CIT6920; 3) OSF SMMC CIRCUMCISION KIT, Pack Number CIT7095; 4) RETINAL INJECTION KIT, Pack Number MNS12465; 5) UCLA - BREAST BIOPSY KIT, Pa
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2626-2024·2024-09-04
Medline Medical Convenience Kits with Syringes Recalled for Leaks and Breakage
Medline Industries recalls 1,679,067 medical convenience kits containing plastic syringes that may leak or break, posing potential risks to patient health.
Product
See RES description
Category
Medical Device
Distribution
0 states
SevereNHTSA·24V097000·2024-09-02
2021-2022 Ford E-350 and E-450 Power Steering Fluid Loss Recall
Ford is recalling certain 2021-2022 E-350 and E-450 vehicles due to a defective power steering connection that may cause loss of power steering fluid and brake assist.
Product
FORD — 2021 FORD E-350
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V094000·2024-09-02
2024 Coachmen Catalina Travel Trailers Recalled for Tire Puncture Risk
Forest River is recalling 2024 Coachmen Catalina and Forest River Aurora travel trailers because the tire may contact the slide adjustment bolt and puncture. A punctured tire can cause loss of vehicle control and increase crash risk.
Product
COACHMEN — 2024 COACHMEN CATALINA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V100000·2024-09-02
Mercedes-Benz recalls 2021-2023 vehicles for ground cable fire risk
Mercedes-Benz USA is recalling 2021-2023 models including AMG GT53, CLS450, E450, and others because the 48-volt ground cable connection may not be tightened properly, risking fire.
Product
MERCEDES-BENZ — 2023 MERCEDES-BENZ AMG GT53
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V108000·2024-09-02
2023 Infiniti QX60 Second-Row Seat May Fail to Lock Properly
The second-row adjustable seat may extend past its stopper and fail to lock in certain 2023 Infiniti QX60 vehicles. This defect could prevent proper occupant restraint during a crash, increasing injury risk.
Product
INFINITI — 2023 INFINITI QX60
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·24350·2024-08-29
HALO 1000 Portable Power Stations Recalled for Fire and Burn Hazards
About 5,740 HALO 1000 Portable Power Stations are recalled because their lithium-ion batteries can overheat and catch fire. One death from smoke inhalation and four fire incidents have been reported.
Product
HALO 1000 Portable Power Stations
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24352·2024-08-29
Glow in Dark Party Supplies Toy Sets Recalled for Battery Ingestion Hazard
Glow in Dark Party Supplies Toy Sets sold on Amazon contain button cell batteries in Bunny Ears Headbands that can be easily accessed by children, posing a serious ingestion hazard. The sets violate federal battery-operated toy regulations.
Product
Glow in Dark Party Supplies Toy Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24351·2024-08-29
Fisher-Price Dumbbell Toy Recalled for Choking Hazard
Fisher-Price is recalling a plastic dumbbell toy sold in the Baby Biceps Gift Set because the gray caps on the ends can come off, posing a choking hazard to infants. The firm has received seven reports of the ends coming off but no injuries have been reported.
Product
Dumbbell toy sold with Baby Biceps Gift Set
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2636-2024·2024-08-28
McGrath Mac Video Laryngoscope battery depletion may cause thermal event and explosion
McGrath Mac Video Laryngoscope devices may experience battery management system failures causing batteries to deplete below design thresholds, potentially resulting in thermal events and explosions.
Product
McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2637-2024·2024-08-28
McGRATH MAC EMS Video Laryngoscope Battery Management System Recall
Covidien is recalling McGRATH MAC EMS Video Laryngoscopes due to a battery management system defect that may deplete below design specifications, creating risk of thermal events and explosion. About 10,449 units were distributed worldwide.
Product
McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , Non-Sterile, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0641-2024·2024-08-28
Acetaminophen Aspirin Caffeine Tablets Recalled for Missing Drug Facts Labels
Aurohealth LLC is recalling Acetaminophen, Aspirin and Caffeine tablets because some bottles are missing the manufacturer's label containing drug facts information. Affected product was distributed in NJ, NY, and PA.
Product
ACETAMINOPHEN ASPIRIN AND CAFFEINE — ACETAMINOPHEN ASPIRIN AND CAFFEINE (ACETAMINOPHEN, ASPIRIN AND CAFFEINE)
Category
Drug
Distribution
3 states
SevereFDA (Food)·F-1788-2024·2024-08-28
Meijer Dunking Cookies Recalled for Undeclared Milk Allergen
Meijer Inc is recalling Meijer Dunking Cookies Chocolate Chip (10 oz) due to undeclared milk. The product poses a risk to consumers with milk allergies.
Product
MEIJER DUNKING COOKIES CHOCOLATE CHIP, 10oz in clear plastic container. UPC 7-13733-71297-2
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-2587-2024·2024-08-28
ClotTriever XL Catheter instructions updated to prevent device entrapment and embolism
Inari Medical has updated instructions for the ClotTriever XL Catheter (30 mm) to prevent device entrapment and pulmonary embolism. Approximately 2,488 units distributed worldwide are affected.
Product
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0635-2024·2024-08-28
FDA Recalls Acetaminophen Injection Due to Labeling Mix-up
Hikma Pharmaceuticals is recalling Acetaminophen Injection because bags of Dexmedetomidine HCl were found packaged inside Acetaminophen-labeled overWraps. The error could result in patients receiving the wrong intravenous medication.
Product
ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-0638-2024·2024-08-28
FDA Class I Recall: B. Braun Sodium Chloride Injection for Particulate Matter
B. Braun Medical Inc. is recalling 63,444 containers of 0.9% Sodium Chloride Injection USP nationwide due to the presence of particulate matter. This intravenous medication may pose a serious health risk if administered to patients.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2664-2024·2024-08-28
Ophthalmic knife sharpness defect recalled for increased complaints
Alcon recalls 3,419 ophthalmic knives due to increased complaints about blade sharpness. The Class II recall affects the ClearCut SB INTREPID 2.2 ANG and related models distributed nationwide and internationally.
Product
Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number: 8065992561 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide

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11051–11075 of 27647