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

51–75 of 594

CriticalFDA (Devices)·Z-0005-2025·2024-10-16
Z-800 Infusion System Recalled for Air-in-Line Software Algorithm Defect
Zyno Medical LLC is recalling the Z-800 Infusion System due to a defect in the air-in-line software algorithm. Approximately 34,994 units distributed nationwide are affected by this Class I FDA recall.
Product
Z-800 Infusion System, Model Numbers Z-800, Z-800F, Z-800W, Z-800WF; Software Version: Z-800 6.1.01 and 6-1.07z; Z-800F 4.1.02 and 4.1.08z; Z-800W 3.1.32 and 3.1.64z, Z-800WF 3.1.32 and 3.1.64z
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·25009·2024-10-10
Fisher-Price Recalls 2.1 Million Snuga Infant Swings for Suffocation Risk
Fisher-Price is recalling approximately 2.1 million Snuga Infant Swings due to suffocation hazard when the product is used for sleep or bedding is added. Five deaths have been reported between 2012 and 2022.
Product
All Models of Fisher-Price Snuga Swings
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1838-2024·2024-10-09
Kandy brand whole cantaloupes recalled for possible Salmonella contamination
Eagle Produce LLC is recalling Kandy brand whole cantaloupes due to possible Salmonella contamination. The recalled product (224 cases of 9-count boxes) was distributed to Michigan, Missouri, Ohio, Texas, and Virginia.
Product
Whole cantaloupe, brand name Kandy, packed in a corrugated box, 9 count
Category
Food
Distribution
5 states
CriticalFDA (Devices)·Z-3084-2024·2024-09-25
Baxter pharmaceutical compounding inlets recalled for particulate matter contamination
Baxter is recalling EXACTAMIX compounding device inlets due to particulate matter observed in sterile fluid pathways before use. Approximately 5.8 million units affected worldwide.
Product
Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175, for use in a pharmaceutical compounding device
Category
Medical Device
Distribution
0 states
CriticalCPSC·24359·2024-09-12
About 866,000 AirJet and HydroJet Spa Pumps Recalled for Fire Hazard
AirJet and HydroJet spa pumps can overheat and ignite, posing a fire hazard. One death has been reported, and consumers should stop using the pumps immediately.
Product
AirJet and HydroJet Spa Pumps
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1762-2024·2024-09-11
JFE Pico de Gallo Classic Products Recalled for Listeria Contamination
JFE FRANCHISING INC is recalling Pico de Gallo Classic products in Kentucky, Michigan, Ohio, and West Virginia due to potential Listeria monocytogenes contamination. Consumers should not consume affected products and should return them to the place of purchase or discard them.
Product
Pico de Gallo Classic Hot - 14 oz 639123880116 Pico de Gallo Classic Medium - 14 oz 639123880093 Pico de Gallo Classic Mild - 14 oz 639123880109 Plastic Clam-Shell Container
Category
Food
Distribution
4 states
CriticalFDA (Devices)·Z-2943-2024·2024-09-11
Trilogy Evo Ventilator Software Update for Identified Safety Issues
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for the Trilogy Evo Universal Ventilator to address safety issues identified in earlier recalls. Affected units should implement the update.
Product
Trilogy Evo Universal Ventilator, Model No. DS2000X11B
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2592-2024·2024-09-04
PORTEX Bivona Tracheostomy Tubes Recalled for Flange Tearing Defect
Smiths Medical is recalling PORTEX Bivona Tracheostomy Tubes because the securement flange may tear due to a manufacturing defect, risking loss of airway securement.
Product
PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACHEOSTOMY TUBE 2.5FLEXTEND PLUS , Product Code/List Number/Item Code 60NFP25; b) NEONATAL TRACHEOSTOMY TUBE 3.0FLEXTEND PLUS , Product Code/List Number/Item Code 60NFP30; c) NEONATAL TRACHEOSTOMY TUBE
Category
Medical Device
Distribution
0 states
CriticalFDA (Devices)·Z-2606-2024·2024-09-04
Smiths Medical Bivona Neonatal Tracheostomy Tubes Recalled for Flange Tear
Smiths Medical recalls PORTEX Bivona Neonatal Tracheostomy Tubes due to manufacturing defect that may cause securement flange to tear, compromising tube stability.
Product
PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N025; b) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N030; c) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N035
Category
Medical Device
Distribution
0 states
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
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
CriticalFDA (Food)·F-1707-2024·2024-08-21
Freshire Farms jalapenos recalled for potential Listeria monocytogenes contamination
Freshire Farms jalapenos packaged in 8-ounce bags are being recalled due to potential contamination with Listeria monocytogenes. The recall affects 2,298 cases distributed across nine states.
Product
Freshire Farms - Jalapenos packaged in plastic bags at 8oz, 18 bags per case
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-1709-2024·2024-08-21
Green peppers recalled due to potential Listeria contamination
RS Hanline and Company Inc is recalling Freshire Farms green peppers due to potential Listeria monocytogenes contamination. The recall affects 850 cases distributed across nine states.
Product
Freshire Farms - Green Peppers packaged in plastic bags containing 3 peppers, 16 bags per case
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-1677-2024·2024-08-14
Wiers Farm Poblano Peppers recalled for Listeria contamination
Wiers Farm Inc is recalling Poblano peppers in 16oz bags due to Listeria monocytogenes contamination. The product was distributed across multiple states.
Product
Wiers Farm - Poblano packaged in 16oz plastic bag - 10 bags in a case
Category
Food
Distribution
18 states
CriticalFDA (Devices)·Z-2446-2024·2024-08-14
Puritan Bennett 500 Series Ventilators recalled due to volatile organic compound release
Covidien recalls 34,642 Puritan Bennett 500 Series Ventilators due to release of volatile organic compound (2-propanol, 1,3-dichloro) from gas pathway components during prolonged use beyond 10 years.
Product
Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560 VENTILATOR EU-DIV/4096600-01, PURITAN BENNETT 560 VENTILATOR JAPAN/4096600-02, PURITAN BENNETT 560 VENTILATOR APAC/4096600-03, Puritan Bennett 560 Ventilat
Category
Medical Device
Distribution
34 states
CriticalFDA (Food)·F-1695-2024·2024-08-14
Wiers Farm Tomatillos Recalled Due to Listeria Monocytogenes Contamination
Wiers Farm is recalling 1,467 cases of tomatillos due to Listeria monocytogenes contamination. Affected lot numbers 240705-240712 were distributed across 17 states.
Product
Wiers Farm - Tomatillos packaged in 1lb cartons - case size dependent on customer
Category
Food
Distribution
18 states
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
CriticalFDA (Food)·F-1671-2024·2024-08-14
Palmer Candy and Meijer Popcorn Products Recalled for Salmonella
Palmer & Company is recalling Palmer Candy Drizzled Caramel Corn and Meijer Drizzled Caramel Popcorn Snack Bowls due to potential Salmonella contamination. Products were distributed nationwide in the United States and Canada.
Product
1. Palmer Candy Drizzled Caramel Corn, Item 19271, Net Wt. 16/5oz tubs, UPC 77343 19271 2. Meijer Drizzled Caramel Popcorn Snack Bowl, Net Wt. 12oz, UPC 60236 18830, 8/12oz case
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1678-2024·2024-08-14
Cubanelle Peppers from Wiers Farm Recalled for Listeria Contamination
Wiers Farm is recalling specific lots of cubanelle peppers due to potential Listeria monocytogenes contamination. The affected products were distributed across 18 states.
Product
Wiers Farm - Cubanelle packaged in 16oz plastic bag - 10 bags in a case
Category
Food
Distribution
18 states
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-1645-2024·2024-08-14
Bazzini Raw Almond Butter Recalled for Undeclared Peanuts
Bazzini LLC is recalling 684 jars of Bazzini Raw Almond Butter (Lot code 2E136) due to undeclared peanuts, posing a serious risk to peanut-allergic consumers. The affected product was distributed to retailers in New York.
Product
Bazzini Raw Almond Butter Net Wt. 16 oz (454g) UPC Code 7506284009. Packaged in clear plastic jars with plastic white lids. 12 jars per case
Category
Food
Distribution
1 state
CriticalFDA (Food)·F-1683-2024·2024-08-14
Wiers Farm Organic Yellow Squash Recalled for Listeria Contamination
Wiers Farm Inc is recalling organic yellow squash in 2-count trays due to Listeria monocytogenes contamination. The recall affects 54 cases distributed across 17 states.
Product
Wiers Farm - Organic Yellow Squash packaged into 2 count trays - cases dependent on customer
Category
Food
Distribution
18 states
CriticalFDA (Food)·F-1540-2024·2024-08-07
Diamond Shruumz Gummies recalled for toxic muscimol levels
Diamond Shruumz Gummies Mega/Extreme Dose Peach Paradise contain toxic levels of muscimol. The FDA is recalling all 248,007 units distributed nationwide.
Product
Diamond Shruumz Gummies - Mega/Extreme Dose Peach Paradise UPC 810133320384
Category
Food
Distribution
51 states
CriticalFDA (Food)·F-1535-2024·2024-08-07
Diamond Shruumz Gummies Recalled for Toxic Levels of Muscimol
Diamond Shruumz Gummies (Micro Dose Sour Peach Apple) manufactured by Prophet Premium Blends, LLC, are being recalled by the FDA due to toxic levels of muscimol. The Class I recall affects approximately 248,007 products distributed nationwide.
Product
Diamond Shruumz Gummies - Micro Dose Sour Peach Apple UPC 755003861386
Category
Food
Distribution
51 states
CriticalFDA (Drugs)·D-0620-2024·2024-08-07
Dietary Supplement Recalled for Undeclared Diclofenac and Omeprazole
SoloVital's Umary Hyaluronic Acid supplement was recalled because FDA testing found it contains undeclared Diclofenac and Omeprazole. The product, marketed without approved NDA/ANDA, affected 1,331 bottles distributed nationwide.
Product
Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
Category
Drug
Distribution
Distributed nationwide

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51–75 of 594