The Recall Desk

State

Tennessee product recalls

73,106 recalls have nationwide distribution and so reach Tennessee. 7,851 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,327
Severe
1,665
Most recent
2026-09-23

Of the 7,851 recalls naming Tennessee we have scored against our rubric, 1,327 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,665 (21%) are Severe.

These figures cover only the 7,851 recalls whose distribution notice names Tennessee specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10776–10800 of 80957

  • 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-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-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-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
  • HighFDA (Food)·F-1725-2024·2024-08-14

    Concha Mexicana Pastries Recalled Due to Undeclared Soy Allergen

    Panaderia Guatemex is recalling Concha Mexicana pastries due to undeclared soy allergen. Consumers with soy allergies should not consume this product.

    Product
    Panaderia Guatemex - Concha Mexicana packaged in plastic bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1716-2024·2024-08-14

    Panaderia Guatemex Corona Bread Recalled for Undeclared Soy Allergen

    Panaderia Guatemex is recalling Corona brand bread packaged in plastic bags due to undeclared soy allergen. The affected product was distributed in Georgia, Kentucky, and Tennessee.

    Product
    Panaderia Guatemex - Corona packaged in plastic bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2509-2024·2024-08-14

    Philips IntelliVue Patient Monitors with disabled monitoring software options

    Philips IntelliVue Patient Monitors (MX400/450/500/550) with software versions L.x or M.x lack required monitoring capabilities due to removed software entitlements. The missing features could lead to incorrect or delayed patient treatment.

    Product
    IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866062. 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 (Devices)·Z-2514-2024·2024-08-14

    Diagnostic Test Kits Recalled for False Vibrio Results With Certain Transport Medium

    BioFire Diagnostics is recalling gastrointestinal diagnostic test kits due to false positive Vibrio results when used with certain transport mediums.

    Product
    BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0104 (6 kit test) The BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2539-2024·2024-08-14

    Medical Device Hookup Instructions Contain Errors Affecting Endoscope Disinfection

    Steris Corporation recalls certain automated endoscope reprocessor hookups due to incorrect instructions in product documentation. Improper hookup connection could prevent proper endoscope disinfection, risking patient infection.

    Product
    Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER ) and endoscopes, which allow perfusion of liquids dispensed by the AER to contact and high-level disinfect the channels of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2518-2024·2024-08-14

    Gyn Laparoscopy Kits Recalled Due to Inadequate Sterilization Process

    American Contract Systems is recalling 29 gynecological laparoscopy surgical kits due to insufficient aeration during sterilization, which may compromise sterility and increase infection risk for patients.

    Product
    American Contract Systems Gyn Laparoscopy convenience kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2492-2024·2024-08-14

    Automated Medication Cabinet Software Bug May Print Wrong Bin Labels

    CareFusion's BD PYXIS MEDBANK medication dispensing cabinets (software 3.9.1.9) have a software defect that may cause restock labels to print incorrect medication bin locations, creating a risk of medication dispensing errors.

    Product
    BD PYXIS MEDBANK TWR MN CR-14HH-P, REF: 169-86 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide