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

901–925 of 5642

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 (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
SevereCPSC·24347·2024-08-22
Head Rush Technologies TRUBLUE Speed Auto Belay Devices Fall Hazard
Head Rush Technologies is recalling about 220 TRUBLUE Speed Auto Belay Devices because the backup brake can fail to activate, posing a fall hazard and risk of serious injury or death. Consumers should immediately stop using the devices and contact the manufacturer for a free inspection and repair.
Product
TRUBLUE Speed Auto Belay Devices
Category
Consumer Product
Distribution
Distributed nationwide
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-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
SevereFDA (Food)·F-1735-2024·2024-08-21
Lunds & Byerlys Guacamole Dip Recalled for Listeria Risk
Metro Produce Distributors is recalling 66 units of Lunds & Byerlys Pico de Gallo/Guacamole Dip distributed in Minnesota due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
Product
Lunds & Byerlys Pico de Gallo / Guacamole Dip, Net Wt 18 oz (510g). UPC 0 72431-02993 6. Keep Refrigerated.
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2449-2024·2024-08-21
Plum 360/A+ Spare Battery Defect Causes Accelerated Capacity Loss
ICU Medical is recalling 130,826 units of Plum 360/A+ spare batteries due to a manufacturing defect that causes earlier-than-expected battery capacity loss and reduced runtime.
Product
Plum 360/A+ spare batteries. Item Number: SUB0000864.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1712-2024·2024-08-21
Green Peppers Recalled Due to Potential Listeria Contamination
RS Hanline and Company Inc is recalling green peppers due to potential Listeria monocytogenes contamination. The recall affects peppers distributed across nine states.
Product
Green Peppers packaged as whole 10lb carton, whole 20lb carton, whole 5lb carton
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1739-2024·2024-08-21
Van Leeuwen Pumpkin Cinnamon Roll frozen dessert recalled for undeclared peanuts
Van Leeuwen Ice Cream is recalling Pumpkin Cinnamon Roll non-dairy frozen dessert (14 oz) due to undeclared peanuts. The allergen poses serious risk to consumers with peanut allergies.
Product
VEGAN OAT; Van Leeuwen PUMPKIN CINNAMON ROLL; NON-DAIRY FROZEN DESSERT 14 oz, (414 ml); Est. Brooklyn 2008 ingredients: oat milk (water, oats) coconut cream, cane sugar, brown sugar, unbleached wheat flour, tapioca syrup, pumpkin puree, coconut oil, cocoa butter, water, ginger,
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1708-2024·2024-08-21
Freshire Farms Green Beans Recalled for Potential Listeria Contamination
RS Hanline and Company Inc is recalling Freshire Farms Green Beans due to potential Listeria monocytogenes contamination. Approximately 1150 cases were distributed across nine states.
Product
Freshire Farms - Green Beans packaged in plastic bags at 1lb, 14 bags per case
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1732-2024·2024-08-21
Lunds & Byerlys Fresh Guacamole Dip Recalled for Listeria Contamination
Metro Produce Distributors is recalling Lunds & Byerlys Fresh Guacamole Dip due to potential Listeria monocytogenes contamination. The affected product has a Use By date of 02-AUG-24 and was distributed in Minnesota.
Product
Lunds & Byerlys Fresh Guacamole Dip, Net Wt 14 oz (396g). UPC 0 72431-66072 6. Keep Refrigerated.
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2447-2024·2024-08-21
Plum 360 Infusion Battery Recall Due to Manufacturing Defect
ICU Medical is recalling Plum 360 Infusion System replacement batteries due to a manufacturing defect that may cause loss of capacity and decreased runtime earlier than expected. Approximately 11,961 units were distributed worldwide.
Product
Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010. Product description is PLUM 360 Infuser. OUS units marketed with the following descriptions: Bomba de infusi¿n Plum 360 compatible con el software ICU Medical MedNet, Plum 360 Inf
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1736-2024·2024-08-21
Lunds & Byerlys Deli Guacamole Recalled for Listeria Contamination
Lunds & Byerlys Deli Guacamole (Item 85999, 56 oz) may be contaminated with Listeria monocytogenes. Twenty-eight units with a Use By date of 02-AUG-24 were distributed in Minnesota.
Product
Lunds & Byerlys Deli Guacamole, Item 85999. Net Wt 56 oz. Keep Refrigerated.
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2543-2024·2024-08-21
RMU-2000 Automated Chest Compression Device Recalled Due to Motor Failure
Defibtech is recalling the RMU-2000 Automated Chest Compression Device because a motor defect may cause the device to stop delivering compressions, potentially delaying critical therapy and resulting in patient injury or death.
Product
RMU-2000 Automated Chest Compression Device
Category
Medical Device
Distribution
5 states
SevereFDA (Food)·F-1740-2024·2024-08-21
North Fish USA Recalls Cold Smoked Capelin Due to Botulism Risk
North Fish USA is recalling Cold Smoked Capelin packages due to potential Clostridium botulinum contamination in uneviscerated fish. The affected products were distributed in Georgia and New York.
Product
Cold Smoked Capelin, 9-ounce packages, plastic trays, 34 packages per case (Best By Date:07.13.2024), 18 packages per case (Best Buy Date: 01.05.2025), UPC code4811527003360, Keep Frozen,UPC code 4811527003360
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1728-2024·2024-08-21
Foppen Smoked Norwegian Salmon Slices Recalled for Potential Listeria Contamination
Foppen Smoked Norwegian Salmon Slices (8.1oz vacuum foil packages) are recalled due to potential contamination with Listeria monocytogenes. The recall affects 747 cases distributed across 15 U.S. states.
Product
Foppen Smoked Norwegian Salmon Slices - Toast Size, packaged in 8.1oz vacuum foil, packaged within cardboard envelope. Keep Refrigerated at 38F or below.
Category
Food
Distribution
15 states
SevereFDA (Food)·F-1703-2024·2024-08-21
Boars Head Ham Recalled Due to Potential Listeria Monocytogenes Contamination
Publix Super Markets is recalling 2,786 units of Boars Head Grab and Go Wedge Ham products due to potential Listeria monocytogenes contamination. The affected products were sold at retail locations in Florida and Georgia.
Product
Boars Head Grab and Go Wedge Ham, Smoke Master Black Forest Ham, Grab and Go Sandwich, NET WT. 7.5 OZ (213 g), Plastic Container, KEEP REFRIGERATED
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-2448-2024·2024-08-21
Plum A+ and Plum A+3 Infusion Pump Batteries Recalled for Capacity Loss Defect
ICU Medical is recalling Plum A+ and Plum A+3 infusion pump batteries due to a manufacturing defect that may cause premature capacity loss and reduced runtime. Approximately 14,744 units were distributed worldwide.
Product
Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum A+ & Plum A+3 Infusion Systems, Pump List Numbers: 11005, 11971, 12391, 12618, 20678, 20679, 20792, 60529, 12348, 11973. OUS units marketed with the following descriptions: Plum A+ Mednet TM Firmware New 1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1734-2024·2024-08-21
Lunds & Byerlys Smokin' Guacamole Dip recalled due to Listeria contamination
Metro Produce Distributors is recalling Lunds & Byerlys Smokin' Guacamole Dip due to possible Listeria monocytogenes contamination. The 10 oz product was distributed in Minnesota.
Product
Lunds & Byerlys Smokin' Guacamole Dip, Net Wt 10 oz (283g). UPC 0 72431-66130 3. Keep Refrigerated.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1733-2024·2024-08-21
Lunds & Byerlys Spicy Guacamole Dip recalled due to Listeria contamination
Metro Produce Distributors is recalling 121 units of Lunds & Byerlys Spicy Guacamole Dip because it may be contaminated with Listeria monocytogenes. The affected product was distributed in Minnesota.
Product
Lunds & Byerlys Spicy Guacamole Dip, Net Wt 10 oz (283g). UPC 0 72431-66128 0. Keep Refrigerated.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1711-2024·2024-08-21
Poblano Peppers Recalled Due to Potential Listeria Contamination
RS Hanline and Company Inc is recalling Poblano peppers in multiple package formats due to potential Listeria monocytogenes contamination. The affected product was distributed across nine U.S. states.
Product
Poblano packaged as 5lb half sliced with 2 bags per case, 5lb fourth diced with 2 bags per case, 5lb half diced with 2 bags per case
Category
Food
Distribution
0 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 (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-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 (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

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901–925 of 5642