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 the agency’s own highest classification or reported deaths or serious injuries, 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

11476–11500 of 89679

SevereFDA (Food)·F-1656-2024·2024-08-14
Yogurt-Covered Pretzel Recall Due to Potential Salmonella Contamination
Palmer & Company is recalling multiple yogurt-covered pretzel products distributed nationwide due to potential salmonella contamination. Consumers should not consume these products.
Product
1. Palmer Candy Classic Yogurt Pretzels, Net Wt 28 lbs, UPC 77232 10847 2. Sweet Smiles Yogurt Covered Pretzels, Net Wt. 3.25oz, UPC 77232 13641, 8/3.25oz case 3. Sconza Chocolates Yogurt Pretzels, Net Wt 14lbs, UPC 004166882015 4. Sunny Select Vanilla Yogurt Coated Pretzels…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1697-2024·2024-08-14
Wiers Farm Butternut Squash Recalled for Listeria Monocytogenes
Wiers Farm Inc is recalling Butternut Squash in 1-pound cartons due to potential Listeria monocytogenes contamination. Lot numbers 240705 through 240712 are affected.
Product
Wiers Farm - Butternut Squash packaged in 1lb cartons - case size dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1689-2024·2024-08-14
Green Bell Peppers Recalled for Listeria monocytogenes Contamination
Wiers Farm green bell peppers packaged in 1-pound cartons are being recalled due to potential Listeria monocytogenes contamination. Affected lot numbers are 240705 through 240712, distributed across 17 states.
Product
Wiers Farm - Green Bell Pepper packaged into 1lb carton - cases size dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1688-2024·2024-08-14
Wiers Farm Habanero Peppers Recalled for Listeria Contamination
Wiers Farm Inc is recalling habanero peppers sold in 1-pound cartons across 17 states due to potential Listeria monocytogenes contamination. The recall involves 441 cases with lot numbers 240705 through 240712.
Product
Wiers Farm - Habanero Peppers packaged into 1lb carton - 3lb per case
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1647-2024·2024-08-14
SAVPAK Duro Rueda 8oz Contains Undeclared Wheat Allergen
SAVPAK Duro Rueda 8oz packages distributed in Texas contain undeclared wheat allergen. Consumers with wheat allergies or celiac disease should not consume this product.
Product
SAVPAK Duro Rueda 8oz, plastic bag, DISTRIBUTED BY: Southcoast Produce Inc. Dallas, Texas 75215; UPC 29661 00073
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1646-2024·2024-08-14
SAVPAK Duro Plastic Bags Recalled for Undeclared Wheat Allergen
SAVPAK Duro 8oz plastic bags distributed in Texas are being recalled because they contain wheat that is not declared on the label. Consumers with wheat allergies should stop using the product immediately.
Product
SAVPAK Duro 10x10, 8oz plastic bag, DISTRIBUTED BY: Southcoast Product Inc. Dallas, Texas 75215; UPC 29661 00076.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1694-2024·2024-08-14
Wiers Farm Plain Parsley Recalled Due to Listeria Contamination
Wiers Farm Inc is recalling 148 cases of Plain Parsley due to potential Listeria monocytogenes contamination. The affected product was distributed across 17 states.
Product
Wiers Farm - Plain Parsley packaged in 1lb cartons - 15 cartons per case
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1680-2024·2024-08-14
Wiers Farm Serrano Peppers recalled for Listeria monocytogenes contamination
Wiers Farm Inc is recalling Serrano Peppers sold in 4oz bags due to potential Listeria monocytogenes contamination. The recall affects approximately 1,708 cases distributed across 16 states.
Product
Wiers Farm - Serrano Peppers packaged in 4oz plastic bag - 5lbs per case
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1684-2024·2024-08-14
Organic Zucchini Squash Recalled Due to Listeria Contamination
Wiers Farm is recalling organic zucchini squash due to potential Listeria monocytogenes contamination. The recall affects 337 cases across 17 states with lot numbers 240705 through 240712.
Product
Wiers Farm - Organic Zucchini Squash packaged into 2 count trays - cases dependent on customer
Category
Food
Distribution
18 states
SevereFDA (Food)·F-1687-2024·2024-08-14
Cilantro Recalled Due to Listeria Monocytogenes Contamination
Wiers Farm is recalling cilantro packaged in 1-pound cartons due to potential Listeria monocytogenes contamination. The affected product was distributed to 2,798 cases across 16 U.S. states.
Product
Wiers Farm - Cilantro packaged into 1lb cartons - 30 or 60 cartons per case dependent on customer
Category
Food
Distribution
18 states
HighFDA (Food)·F-1722-2024·2024-08-14
Panaderia Guatemex Pegado Bread Recalled for Undeclared Soy Allergen
Panaderia Guatemex is recalling Pegado bread packaged in plastic bags due to undeclared soy allergen. Affected products were distributed in Georgia, Kentucky, and Tennessee.
Product
Panaderia Guatemex - Pegado packaged in plastic bag
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2483-2024·2024-08-14
MRI System Software Error Can Overheat Patient Implants
GE Medical Systems recalled three SIGNA 7.0T MRI systems due to a software error that can exceed preset safety limits during imaging, potentially overheating implants in patients under certain conditions.
Product
SIGNA 7.0T, with affected software versions: 7T29.1, MR30.1; Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2508-2024·2024-08-14
Philips IntelliVue Patient Monitor Software Missing Critical Entitlements
Philips IntelliVue Patient Monitor models with software L.x and M.x lack critical monitoring capabilities due to a software update. This could result in incorrect or delayed patient treatment.
Product
IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866060. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0634-2024·2024-08-14
Gabapentin 600 mg Tablets Recalled Due to Metformin Contamination
Granules Pharmaceuticals Inc. is recalling Gabapentin Tablets 600 mg nationwide after fused Metformin ER tablets were found in bottles, creating a risk of unintended medication exposure.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2491-2024·2024-08-14
BD PYXIS MEDBANK Cabinet Software Causes Incorrect Medication Labels
FDA recall of BD PYXIS MEDBANK automated medication dispensing cabinets due to a software defect that prints incorrect bin information on restock labels, potentially leading to medication identification errors.
Product
BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P, REF: 169-85 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1648-2024·2024-08-14
Premo King Club Footlong Sandwiches Recalled for Potential Salmonella Contamination
Lipari Foods is recalling Premo King Club Footlong sandwiches (UPC 612510094259) due to potential Salmonella contamination. The recall affects 216 cases distributed to retailers across 16 states; consumers should discard the product or return it to the store.
Product
Premo King Club Footlong 11.5oz, clear plastic, UPC 612510094259, 4 retail packages per wholesale case
Category
Food
Distribution
16 states
HighFDA (Devices)·Z-2496-2024·2024-08-14
Automated Medication Dispensing Cabinet Software Issue with Incorrect Bin Labeling
BD PYXIS MEDBANK automated medication dispensing cabinets with software version 3.9.1.9 may generate incorrect bin location labels during restocking. This could cause medications to be placed in wrong storage locations.
Product
BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P, REF: 169-91 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1719-2024·2024-08-14
Panaderia Guatemex Sheca Anis Bread Recalled for Undeclared Soy Allergen
Panaderia Guatemex is recalling Sheca Anis bread products due to undeclared soy allergen. The recall affects 170 bags distributed in Georgia, Kentucky, and Tennessee.
Product
Panaderia Guatemex - Sheca Anis packaged in plastic bag
Category
Food
Distribution
3 states
HighNHTSA·24V610000·2024-08-14
Holiday Rambler Admiral motorhomes recalled for missing GFCI outlet protection
Certain 2019-2025 Holiday Rambler Admiral and other RVs have exterior patio outlets lacking GFCI protection when powered by generator or shore cord, increasing electrical shock risk. Dealers will install GFCI devices free of charge.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, ADMIRAL, ECLIPSE, FLEX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1718-2024·2024-08-14
Panaderia Guatemex Besos Bakery Products Recalled for Undeclared Soy
Panaderia Guatemex is recalling 170 bags of Besos packaged bakery products distributed in Georgia, Kentucky, and Tennessee because they contain undeclared soy, a known allergen that poses a risk to consumers with soy allergies.
Product
Panaderia Guatemex - Besos packaged in plastic bag
Category
Food
Distribution
3 states
HighFDA (Food)·F-1664-2024·2024-08-14
Palmer Patriotic White Fudge Cookies Recalled for Potential Salmonella
Palmer & Company is recalling Palmer Patriotic White Fudge Cookies in 7oz and 13.5oz sizes due to potential salmonella contamination. Affected products were distributed nationwide in the United States and Canada.
Product
1. Palmer Patriotic White Fudge Cookies, Net Wt. 7oz, UPC 7723237084, 16/7oz case 2. Palmer Patriotic White Fudge Cookies, Net Wt. 13.5 oz, UPC 7723237085, 8/13.5oz case
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1727-2024·2024-08-14
Panaderia Guatemex Roscas Recalled for Undeclared Soy Allergen
Panaderia Guatemex is recalling 170 bags of Roscas due to undeclared soy allergen. The product was distributed in Georgia, Kentucky, and Tennessee.
Product
Panaderia Guatemex - Roscas packaged in plastic bag
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2534-2024·2024-08-14
Philips Azurion X-ray System: Potential Loss of Imaging Functionality
The Philips Azurion Interventional Fluoroscopic X-ray System may lose imaging functionality or experience longer restart times. The FDA is recalling approximately 3,011 units of this device worldwide.
Product
Philips Azurion Interventional Fluoroscopic X-ray System with Software Version Number: R1.0, R1.1, R1.2- Intended for Image guidance in diagnostic, interventional, and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2475-2024·2024-08-14
GE SIGNA MR355 MRI System Recalled for Potential Implant Overheating Risk
GE SIGNA MR355 MRI systems running software versions SV25.5 or SV25.6 may cause implant overheating in certain scanning conditions. Risk occurs when using specific imaging sequences with the Optimized T2 FLAIR feature disabled.
Product
SIGNA MR355, with affected software versions: SV25.5, SV25.6; Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2489-2024·2024-08-14
BD PYXIS MEDBANK Automated Cabinet May Print Incorrect Medication Bin Labels
A software issue in the BD PYXIS MEDBANK automated medication dispensing cabinet can cause incorrect bin labels to be printed for restock operations. This could lead to medication administration errors affecting patient safety.
Product
BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

11476–11500 of 89679