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R. Walters Foods, Limited Liability Corporation

R. Walters Foods, Limited Liability Corporation Recalls

All product recalls associated with R. Walters Foods, Limited Liability Corporation.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 2521–2540 of 37661 recalls

Hannaford Seafood Salad (R. Walters Foods) – Undeclared Soy (2024)

Undeclared Allergen

Product contains undeclared hydrolyzed soy protein.

Class IIModerate

FDAOct 29, 2024ME, MA, NH +2 more• R. Walters Foods, Limited Liability Corporation

IBU Tablets (Dr. Reddy's) – Failed Specifications (2024)

Failed Tablet/Capsule Specifications

Class IIILow

FDAOct 29, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

Timolol Maleate Solution (FDC) – Defective Container (2024)

Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle

1...125 126127128 129...1884

Page 127 of 1884Next

Class II

Moderate

FDAOct 29, 2024IN, NJ• FDC Limited

Tomographic Imager (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

Tempus LS-Manual Defibrillator (Remote Diagnostic) – incorrect labeling (2024)

Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.

Low

FDAOct 28, 2024Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

PORTEX Venn Tracheal Tube Introducer (Smiths Medical) – fluid ingress risk (2024)

Smiths Medical has identified a potential for ingress of fluid into the device during reprocessing. The ingress takes place at the rear of the device between the end cap and the tube. This could lead to staining of the device or allowing the fluid to remain in the device. In addition, the Hypochlorite Solution (200ppm) and the 4% Acetic Acid disinfectants recommended in the IFU may be inadequate according to the disinfection standards for this type of device.

Moderate

FDAOct 28, 2024Nationwide• Smiths Medical ASD, Inc.

Discovery MR750w 3.0T Scanner (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

SIGNA Architect AIR MRI (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

AMS Urinary Sphincter Control Pump (Boston Scientific) – mislabeled packaging (2024)

Potential for mislabeled packaging in which a device labeled as a Pressure Regulating Balloon (UPN 72400024) which instead contained a Control Pump (UPN 72400098)

Moderate

FDAOct 28, 2024Nationwide• Boston Scientific Corporation

PORTEX Tracheal Tube Exchange Guide (Smiths Medical) – fluid ingress risk (2024)

Moderate

FDAOct 28, 2024Nationwide• Smiths Medical ASD, Inc.

SIGNA Architect MRI System (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

Moderate

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

2025 Forest River Palomino (Forest River) – LP gas manifold damage (2024)

Fire/Burn Risk

Forest River, Inc (Forest River) is recalling certain 2025 Palomino recreational vehicles. The axle equalizer may contact and damage the LP gas manifold, causing a propane leak.

High

NHTSAOct 25, 2024Nationwide• FOREST RIVER

ENDO Kit (Medline) – missing sterile packaging information (2024)

Identified lots of Olympus product may be missing sterile and manufacturing lot numbers and expiration dates on the sterile packaging. The information can be found on the outer box or zipper bag label. Medline is recalling its kits which utilize affected product as a component.

Moderate

FDAOct 25, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

U-BAKE Chicken Pot Pie (Grand Central) – Undeclared Egg (2024)

Undeclared Egg

Undeclared egg

Class IHigh

FDAOct 25, 2024IN, OR, WA• Grand Central Bakery FRE Co Inc

U-BAKE Marionberry Pie (Grand Central) – Undeclared Egg (2024)

Undeclared Egg

Undeclared egg

Class IHigh

FDAOct 25, 2024IN, OR, WA• Grand Central Bakery FRE Co Inc

U-BAKE Pie Crust (Grand Central) – Undeclared Egg (2024)

Undeclared Egg

Undeclared egg

Class IHigh

FDAOct 25, 2024IN, OR, WA• Grand Central Bakery FRE Co Inc

U-BAKE Apple Pie (Grand Central) – Undeclared Egg (2024)

Undeclared Egg

Undeclared egg

Class IHigh

FDAOct 25, 2024IN, OR, WA• Grand Central Bakery FRE Co Inc

Proteus XR/A Radiographic System (GE Healthcare) – wall stand cable risk (2024)

Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by GE HealthCare have not been replaced at the intervals detailed in the Preventative Maintenance Action List.

Moderate

FDAOct 24, 2024Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China

2025 Spartan Fire Metrostar (Spartan Fire) – mechanical stop missing (2024)

Fire/Burn Risk

Spartan Fire, LLC (Spartan) is recalling certain 2024-2025 Metro Star, FC-94, 2025 Gladiator, and KME Panther vehicles. A missing mechanical stop may allow the cab tilt cylinder to be overextended.

High

NHTSAOct 24, 2024Nationwide• SPARTAN FIRE

Ricky Powersports ATVs (Jiangsu Tiking) – Injury Risk (2024)

Laceration Risk

The recall involves Ricky Powersports Tumble Weed youth ATVs, model TK-110ATV-1, and TGB Blade 600 SE adult ATVs. The Tumble Weed vehicles were sold in burgundy, purple camo, red spider, blue, black, blue spider, black spider, pink camo, leaf camo and army green camo colors and are intended for use by children ages 6 years and older. The model number is printed on an identification plate located at the front of the vehicle between the two front tires. The TGB Blade 600 SE ATVs were sold in black and are intended for use by adults ages 16 years and older. The model number is printed on an identification plate located next to the vehicle's front right tire. Identification plates on both models state "this ATV is subject to Ricky Powersports LLC's action plan approved by the U.S. Consumer Product Safety Commission."

High

CPSCOct 24, 2024Nationwide• Jiangsu Tiking Sports Vehicle Manufacturing Co. Ltd., of China (youth ATV)