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

11926–11950 of 31371

HighFDA (Devices)·Z-2571-2024·2024-08-21
Merit Medical Convenience Kits with Recalled Syringes Pose Leak Risk
Merit Medical is recalling 900 convenience kits containing plastic syringes due to identified leaks, breakage, and quality issues that may pose a risk to patient health.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG (Introducer Catheter), REF: FCL-069-00/A FCL-069-02/A FCL-069-03/A For the introduction of various types of pacing or defibrillator leads and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2572-2024·2024-08-21
Merit Medical Convenience Kits with Defective Syringes Recalled
Merit Medical convenience kits containing defective syringes are being recalled for leaks and breakage that may pose a risk to patient health.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude Prestige (Introducer Catheter), REF: PLP-2505/A PLP-2514/A PLP-2516/A The introduction of various types of pacing/defibrillator leads and catheters i
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2619-2024·2024-08-21
Surgical Lights Recalled for Possible Weld Defect and Frame Detachment
DKK Dai-Ichi Shomei Co., Ltd. is recalling 822 Aurora surgical light heads due to a weld defect that could cause the light head to sag, crack, or detach during use.
Product
Aurora 2 Series, Aurora 7 lighthead; Models: AUR7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2574-2024·2024-08-21
Merit Medical cardiac kits contain plastic syringes with quality defects
Merit Medical convenience kits used in cardiac procedures contain plastic syringes with potential leaks and breakage. The defects were identified following an FDA Safety Alert issued March 19, 2024.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude SNAP (Introducer Catheter kit), REF: For the introduction of various types of pacing leads and catheters to the heart and coronary venous system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2568-2024·2024-08-21
Merit Medical convenience kits recalled for syringe leaks and breakage risks
Merit Medical is recalling convenience kits containing syringes with quality defects including leaks and breakage. The recalled kits may pose a risk to patients undergoing vascular and cardiac procedures.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K22C (Vein Tray Angiography kit), REF: K09T-11796F K12T-01558G K12T-01558H K12T-01822 K12T-01852L K12T-02006J K12T-02054 K12T-02091G K12T-02102B K12T-023
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2621-2024·2024-08-21
Surgical Lighting Equipment Recalled for Cracked Welds and Frame Detachment Risk
Aurora Series surgical light heads are recalled due to cracked welds on the frame. The defects can cause the frame to sag, housing to crack, or the light head to detach.
Product
Aurora 4 Series, Aurora 7 lighthead; Models: AUA7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2583-2024·2024-08-21
HeartMate 3 System Controller membrane may lift, risking fluid damage and device failure
Thoratec LLC is recalling 694 HeartMate 3 System Controllers because the UI membrane may lift along the housing, allowing fluid entry that could damage internal circuits and cause loss of power or pump failure.
Product
HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant Kits or distributed separately: HeartMate 3 LVAS Implant Kit, US, Model: 106524US; HeartMate 3 LVAS Implant Kit, OUS, Model: 106524INT; HeartMate 3 System
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-2617-2024·2024-08-21
Spinal Cord Stimulation Devices May Reset During Charging, Causing Transient Therapy Loss
Boston Scientific spinal cord stimulation implants may reset during routine charging, causing brief loss of therapy. Patients may experience undesired sensations when stimulation restarts, potentially leading to surgical intervention requests.
Product
WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1710-2024·2024-08-21
Jalapeno Peppers from RS Hanline Recalled for Potential Listeria Contamination
RS Hanline and Company Inc is recalling jalapeno peppers due to potential contamination with Listeria monocytogenes. The affected products were distributed across nine states.
Product
Jalapeno peppers packaged as 5lb diced with 2 bags per case, whole as 10lb carton, or whole as 5lb carton
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-2577-2024·2024-08-21
Merit Medical Catheter Kits Recalled for Syringe Leaks and Breakage Issues
Merit Medical convenience kits containing defective plastic syringes are being recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects approximately 4,027 kits distributed nationwide.
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG/Worley advanced CSG (Introducer Catheter kit), REF: FCL-083-02/A WOR-CSG-B1-09/A WOR-CSG-B2-09/A WOR-CSG-BL1-09/A WOR-CSG-E-90/A For the int
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2580-2024·2024-08-21
VITROS Folate Reagent Pack Recalled for Delayed Test Results
Ortho-Clinical Diagnostics is recalling VITROS Folate Reagent Pack due to fibrinogen precipitation causing delayed test results. The recall affects 18,467 units distributed worldwide.
Product
VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1731-2024·2024-08-21
Pariva Marinated Labneh Bites Recalled for Potential Mold Contamination
Pariva LLC recalls Marinated Labneh Bites due to potential mold contamination. Approximately 4,261 units were distributed across seven states.
Product
Pariva Marinated Labneh Bites Rosemary Garlic; NET WT 8 OZ (225g); INGREDIENTS: YOGURT (CULTURED PASTEURIZED GRADE A MILK & CREAM, SKIM MILK, WHEY PROTEIN CONCENTRATE, SALT AND PECTIN), *SUNFLOWER OIL, *EXTRA VIRGIN OLIVE OIL, ROSEMARY SPICES; CONTAINS: MILK, Distributed by, Mayu
Category
Food
Distribution
7 states
ModerateFDA (Devices)·Z-2545-2024·2024-08-21
Discrete Chemistry Analyzer Recalled Due to Carousel Malfunction
Beckman Coulter is recalling 59 units of its Access 2 Immunoassay System Analyzer due to misaligned index wheels causing carousel motion errors that disable the analyzer and cancel patient tests.
Product
Discrete photometric chemistry analyzer for clinical use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1705-2024·2024-08-21
Fox's u-bet Vanilla Syrup Recalled for Potential Microbiological Contamination
SUBCO Foods is recalling Fox's u-bet Vanilla Flavored Syrup due to bloated bottles and elevated pH and water activity levels that indicate potential microbiological contamination and food-borne illness risk.
Product
Fox's u-bet Vanilla Flavored Syrup, 20oz, UPC 070216241016, 12 retail units per wholesale case
Category
Food
Distribution
5 states
ModerateFDA (Drugs)·D-0633-2024·2024-08-21
Hydrocortisone & Acetic Acid Otic Solution Recalled for Potency and Impurity Failures
Taro Pharmaceuticals recalled Hydrocortisone 1% & Acetic Acid 2% Otic Solution (lot AD12890) due to failed impurity specifications and lower-than-established active ingredient levels during stability testing.
Product
Hydrocortisone 1% & Acetic Acid 2% Otic Solution, 10 mL bottle, Rx only, Mfg by: Taro Pharmaceuticals, Inc., Brampton, Ontario, Canada L6T 1C1, Distributed by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-3007-01
Category
Drug
Distribution
0 states
ModerateFDA (Devices)·Z-2638-2024·2024-08-21
PICC Catheter Package Contains Wrong Length, Causing Procedural Delay
Argon Medical Devices recalls PICC catheters that are mislabeled. Packages marked 26G/1.9Fr x 30cm actually contain 26G/1.9Fr x 50cm catheters, which could delay procedures.
Product
L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539
Category
Medical Device
Distribution
4 states
ModerateFDA (Devices)·Z-2622-2024·2024-08-21
Salivary Testosterone ELISA Quality Control Failure Invalidates Test Results
DRG International is recalling Salivary Testosterone ELISA kits (Model SLV-3013) due to out-of-range quality controls that invalidate test runs and delay patient results. The recall affects 257 units distributed nationwide in six states.
Product
Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013 Product Description: An enzyme immunoassay for the quantitative in vitro diagnostic measurement of free active testosterone in saliva.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·24342·2024-08-15
Trader Joe's Mango Tangerine Scented Candles Recalled for Fire Hazard
Trader Joe's recalls 653,000 Mango Tangerine Scented Candles due to fire hazard—flame can spread from wick to wax. Fourteen incidents reported, including minor burns and property damage.
Product
Mango Tangerine Scented Candles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24344·2024-08-15
IKEA VARMFRONT Power Banks Recalled Due to Fire Hazard
IKEA is recalling approximately 1,600 VARMFRONT Power Banks (models E2037 and E2038) because the devices can overheat and pose a fire hazard. No injuries have been reported in the United States.
Product
VARMFRONT Power Banks
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24340·2024-08-15
Mamibaby and Cosy Nation Baby Loungers Recalled for Suffocation and Fall Hazards
About 32,270 Mamibaby and Cosy Nation baby loungers sold on Amazon.com from June 2023 through June 2024 are being recalled because they violate federal infant sleep product regulations and pose suffocation, fall, and entrapment hazards to infants.
Product
Mamibaby and Cosy Nation Baby Loungers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24341·2024-08-15
ALDI Recalls Ambiano Single Serve Coffee Makers for Burn Hazard
ALDI is recalling about 28,000 Ambiano Single Serve Coffee Makers because the machines can expel hot water from the top, causing burns. ALDI has received 25 reports of this defect, including three burn injuries.
Product
Ambiano Single Serve Coffee Makers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24345·2024-08-15
DeWALT Battery Walk-Behind Mowers Recalled for Laceration Hazard
Stanley Black & Decker is recalling about 46,200 DeWALT Battery walk-behind mowers because water entering the handle support can cause the mower to fail to shut off or start without a key, posing a laceration risk.
Product
DeWALT Battery Push walk-behind mowers and DeWALT Battery Self-Propelled walk-behind mowers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24745·2024-08-15
BJ's Warehouse Recalls Berkley Jensen Gazebos for Roof Panel Hazard
BJ's Wholesale Club is recalling about 32,500 Berkley Jensen gazebos because roof panels can dislodge in high winds, causing injury. The company has reported 137 incidents, including one minor injury.
Product
Berkley Jensen Gazebos
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2442-2024·2024-08-14
Medline Medical Procedure Kits Recalled Due to Defective Plastic Syringes
Medline is recalling over 1.6 million medical procedure kits nationwide and internationally due to plastic syringe defects. The affected kits contain syringes with leaks, breakage, and quality issues that may pose risks to patient health.
Product
Medline procedure kits labeled as: 1) CONTINUOUS BLOCK, Pack Number DYNJRA0960C; 2) COMBINED SPINAL AND EPIDURAL, Pack Number DYNJRA1268C; 3) WAL- UNIVERSAL BLOCK TRAY, Pack Number DYNJRA1638C; 4) BASIC DIAGNOSTIC TRAY, Pack Number DYNJRA1928; 5) PREOP NERVE BLOCK TRAY
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1651-2024·2024-08-14
Shelled walnuts recalled due to Listeria contamination
Stutz Packing Company is recalling 2,538 cases of shelled walnuts due to Listeria contamination. The affected product was distributed in Texas and Arizona.
Product
Shelled Walnuts 1lb package in plastic flexible packaging. 24 packages per case
Category
Food
Distribution
2 states

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11926–11950 of 31371