The Recall Desk

State

Tennessee product recalls

20,187 recalls have nationwide distribution and so reach Tennessee. 0 additional recalls listed Tennessee specifically in their distribution scope.

About recalls in Tennessee

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Tennessee consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

8076–8100 of 20187

  • SevereFDA (Food)·F-1665-2024·2024-08-14

    Palmer Candy Munchy Medley products recalled due to potential salmonella contamination

    Palmer & Company is recalling multiple Munchy Medley candy and snack products nationwide due to potential salmonella contamination. Salmonella can cause serious illness in vulnerable populations.

    Product
    1. Palmer Candy Munchy Medley, Item 38004, Net Wt. 16/6oz bulk case, UPC 77232 38004 2. Palmer Candy Munch Medley, Item 10737, Net Wt. 15 lbs, UPC 77232 10737 3. Casey's Munchy Medley, Sweet & Salty Crunch Mix, Net Wt. 4.25 oz, UPC 98437 26083 6/case 4. Snackin' with the Crew! Mi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0631-2024·2024-08-14

    Acetaminophen tablets incorrectly labeled with aspirin drug facts information

    Some bottles of Acetaminophen Extra Strength 500 mg tablets are labeled with the drug facts information for Aspirin 81 mg tablets. The affected lot is 4138197 (expiration 10/31/2025), distributed nationwide.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1654-2024·2024-08-14

    Al'Fez Natural Tahini Recalled for Potential Salmonella Contamination

    Al'Fez Natural Tahini in 5.6oz glass jars is being recalled due to potential Salmonella contamination. The recall affects 3,522 cases distributed nationwide.

    Product
    Al'Fez Natural Tahini in 5.6oz glass jars, UPC 711464506778
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2443-2024·2024-08-14

    Medline Procedure Kits Recalled Due to Defective Plastic Syringes

    Medline procedure kits containing defective plastic syringes are being recalled nationwide. The syringes may leak, break, or have other quality issues that could pose a risk to patient health.

    Product
    Medline procedure kits labeled as: 1) NEPHROLOGY PACK, Pack Number DYNJ59089; 2) NERVE BLOCK TRAY, Pack Number DYNJRA1221A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1655-2024·2024-08-14

    Palmer Zebra Fudge Cookies recalled for potential salmonella contamination

    Palmer & Company is recalling Palmer Zebra Fudge Cookies due to potential salmonella contamination. The product was distributed nationwide in the United States and Canada.

    Product
    1. Palmer Zebra Fudge Cookies, Enrobed Chocolatey Sandwich Cookies, Net Wt. 7 oz, UPC 77232 37064, distributed in case labeled Chocolate & Frosted Cookies, 16/7oz tubs/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1666-2024·2024-08-14

    FDA Recalls Tiger Treats for Potential Salmonella Contamination

    Palmer & Company is recalling Snackin' With The Crew! Tiger Treats for potential salmonella contamination. The recalled products have best-by dates of 12/18/24 and 12/19/24 and were distributed nationwide in the U.S. and Canada.

    Product
    Snackin' With The Crew! Tiger Treats, Net Wt 8oz., UPC 7723222301, 16/8oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1670-2024·2024-08-14

    Peanut Butter Snack Mix Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Freshness Guaranteed Peanut Butter Snack Mix due to potential salmonella contamination. The recall affects 12oz and 4.5oz packages distributed nationwide in the United States and Canada.

    Product
    1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8/12oz case 2. Peanut Butter Snack Mix, Net Wt 4.5oz to go container, Distributed by: Kwik Trip Inc; UPC 39779 00424, 12/4.5oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • 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, Net
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1659-2024·2024-08-14

    Palmer Candy Cookies & Cream Yummy Chow Recalled for Salmonella Contamination Risk

    Palmer & Company is recalling Palmer Candy Cookies & Cream Yummy Chow (Item 10706) nationwide due to potential salmonella contamination. Consumers should not consume the product.

    Product
    Palmer Candy Cookies & Cream Yummy Chow, Item 10706, Net Wt. 14 lbs, UPC 77232 10706
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1661-2024·2024-08-14

    Sunny Select Strawberry Yogurt Coated Pretzels Recalled for Salmonella Risk

    Palmer & Company is recalling Sunny Select Strawberry Yogurt Coated Pretzels (10 oz, UPC 9848796055) distributed nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Sunny Select Strawberry Yogurt Coated Pretzels, Net Wt. 10 oz, UPC 9848796055, 12/10oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1668-2024·2024-08-14

    Palmer Frosted Munchy Medley Snack Mix Recalled for Salmonella

    Palmer & Company is recalling Palmer Frosted Munchy Medley snack mix nationwide (US and Canada) due to potential salmonella contamination. Consumers should not eat the product and should discard it or return it to where purchased.

    Product
    Palmer Frosted Munchy Medley, A mixture of Sweet & Salty Favorites, Net Wt 15 oz., UPC 77232 37013, 8/15oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1663-2024·2024-08-14

    Palmer Patriotic Munchy Medley Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Palmer Patriotic Munchy Medley candy nationwide in the United States and Canada due to potential salmonella contamination.

    Product
    Palmer Patriotic Munchy Medley, Net Wt 15oz, UPC 7723237060, 12/15oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1658-2024·2024-08-14

    Urge! and Casey's Caramel Pretzels Recalled for Potential Salmonella

    Palmer & Company is recalling Urge! Caramel Swirl Pretzels and Casey's Caramel Swirl Coated Pretzels nationwide due to potential Salmonella contamination.

    Product
    1. Urge! Caramel Swirl Pretzels, White Fudge Coated Pretzel Twists Drizzled in Caramel, Net Wt. 6oz, UPC 39779 00417, 8/6oz case 2. Casey's Caramel Swirl Coated Pretzels, Net Wt. 4 oz., UPC 98437 26082, 6/4oz case
    Category
    Food
    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 flexib
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2536-2024·2024-08-14

    Steris Hookup Model 2-8-540 Documentation Error Risks Improper Endoscope Disinfection

    Steris Hookup Model 2-8-540 instructions were incorrectly documented, potentially preventing proper endoscope disinfection and risking patient infection.

    Product
    Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reprocessor and Advantage Plus" Pass-Thru Automated Endoscope Reprocessor ( AER ) and endoscopes, which allow perfusion of liquids dispensed
    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 diagnost
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2533-2024·2024-08-14

    Verigene Gram Positive Blood Culture Test Recalled for Defective Cartridges

    Luminex recalls approximately 1,100 diagnostic kits due to defective test cartridges that may produce false positive results for Staphylococcus lugdunensis and Enterococcus faecium bacteria.

    Product
    Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2540-2024·2024-08-14

    Olympus Everest Bipolar Cutting Forceps Recalled for Packaging Defects

    Olympus is recalling Everest Bipolar Cutting Forceps surgical instruments due to fractures and breakages in packaging trays and Tyvek covers that may compromise sterility. Affected batches: FR150448, FR154445, FR173022.

    Product
    The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cannula, depending on the model/outer diameter size of the forceps. Coagulation is achieved using electrosurgical energy under visualization. The device is to be used with bipolar outputs of c
    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-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-2501-2024·2024-08-14

    Medication Dispensing Cabinet Software Error Can Print Incorrect Bin Labels

    A software error in CareFusion's BD PYXIS automated medication dispensing cabinet can cause incorrect medication bin numbers to be printed on restock labels, risking medication dispensing errors.

    Product
    BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P, REF: 169-97 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2485-2024·2024-08-14

    Automated medication cabinet software prints incorrect bin labels

    The BD PYXIS MEDBANK MINI automated dispensing cabinet software may print incorrect bin locations on restock labels, potentially causing medications to be placed in wrong locations.

    Product
    BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2494-2024·2024-08-14

    Medication Dispensing Cabinet Software Defect Causes Incorrect Bin Labels

    BD PYXIS automated medication dispensing cabinets contain a software issue that may print incorrect bin locations on restock labels. This could result in medications being placed in the wrong bin during restocking.

    Product
    BD PYXIS MEDBANK TWR MN CR-2HH-6FM, REF: 169-89 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2538-2024·2024-08-14

    Steris Endoscope Reprocessor Hookups: Incorrect Instructions Risk Improper Disinfection

    Steris recalls Hookup Model 2-8-540CAS endoscope reprocessor units due to incorrect instructions that could prevent proper disinfection. Using incorrect hookup connections may lead to patient contamination or infection risk.

    Product
    Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide the interface between an Advantage Plus" Automated Endoscope Reprocessor and Advantage Plus" Pass-Thru Automated Endoscope Reprocessor ( AER ) and endoscopes, which allow perfusion of liquids dispens
    Category
    Medical Device
    Distribution
    Distributed nationwide