The Recall Desk

State

Tennessee product recalls

73,737 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,859
Critical
1,324
Severe
1,973
Most recent
2026-10-28

Of the 7,859 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,973 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30651–30675 of 81596

  • SevereFDA (Devices)·Z-2821-2020·2020-08-26

    Arjo Huntleigh Recalls Citadel Plus Bariatric Bed Frames Due to Melting Cables

    Arjo Huntleigh is recalling 145 Citadel Plus Bariatric Bed Frame Systems because Modular Junction Box cables can melt, potentially affecting bed functionality.

    Product
    Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments. It is not intended for use in the home care environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1160-2020·2020-08-26

    Earth Grown Mocha Fudge Frozen Dessert Recalled for Undeclared Cashews

    Smith Foods Inc. is recalling Earth Grown Mocha Fudge Non-Dairy Frozen Dessert due to undeclared cashews, a major food allergen.

    Product
    Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-1282-2020·2020-08-26

    Kroger Recalls Deli Jarlsberg Jalapeno Dip for Salmonella Risk

    The Kroger Co is recalling Deli Jarlsberg Jalapeno Dip in plastic tubs due to potential contamination with Salmonella Newport.

    Product
    DELI JARLSBERG JALAPENO DIP in plastic tubs, all sizes.
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1161-2020·2020-08-26

    Earth Grown Chocolate Non-Dairy Frozen Dessert Recalled for Undeclared Cashews

    Smith Foods Inc. is recalling Earth Grown brand Chocolate Non-Dairy Frozen Dessert because it contains undeclared cashews, a major food allergen.

    Product
    Earth Grown brand Chocolate Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-1280-2020·2020-08-26

    Kroger Recalls AFIN Jarlsberg Cheese Spread Kits for Salmonella Risk

    The Kroger Co is recalling AFIN Jarlsberg Cheese Spread Kits due to potential contamination with Salmonella Newport. The products were distributed in 20 states.

    Product
    AFIN JARLSBERG CHEESE SPREAD KIT in plastic tubs, all sizes.
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1283-2020·2020-08-26

    Kroger Deli Bacon Chive Jarlsberg Dip Recalled for Salmonella Risk

    The Kroger Co is recalling Deli Bacon Chive Jarlsberg Dip due to potential contamination with Salmonella Newport. Consumers should check sell-by dates and discard the product.

    Product
    DELI BACON CHIVE JARLSBERG DIP in plastic tubs, all sizes.
    Category
    Food
    Distribution
    20 states
  • HighNHTSA·20V504000·2020-08-26

    Volkswagen headlights recalled for misalignment defect in 2020-2021 Atlas models

    Volkswagen is recalling 2020 and 2021 Atlas vehicles due to driver's side headlights that may have been aimed too low during production. This misalignment fails to meet federal safety standards and reduces driver visibility.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V506000·2020-08-26

    Kenworth and Peterbilt trucks recalled for suspension bolt defects

    PACCAR is recalling approximately 1,097 certain 2020-2021 Kenworth and Peterbilt heavy trucks with Watson and Chalin steerable lift axle suspension systems. The pivot bolts may be too short to properly engage the locking nuts, risking separation from the suspension and potential vehicle crashes.

    Product
    KENWORTH — KENWORTH, PETERBILT W900, 567, 365, 367
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1159-2020·2020-08-26

    High Liner Foods Recalls Crab Cakes Due to Undeclared Soy Protein

    High Liner Foods is recalling frozen Maryland-style crab cakes because they contain undeclared hydrolyzed soy protein.

    Product
    HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3 oz***KEEP FROZEN***10004302***PRODUCT OF CHINA***DISTRIBUTED BY: HIGH LINER FOODS< PORTSMOUTH, NY 03801; packaged in 9 lb bulk food service cases
    Category
    Food
    Distribution
    33 states
  • HighCPSC·20172·2020-08-26

    CMP Group Recalls Dock Ladders Due to Sharp Edge Laceration Hazard

    CMP Group is recalling aluminum dock ladders because sharp edges on the steps can cut consumers. About 750 units were sold online from 2017 to 2020.

    Product
    Standoff and Wide Dock Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2828-2020·2020-08-26

    NobelReplace Dental Implant Recall Due to Incorrect Measurement Labeling

    Nobel Biocare is recalling 188 NobelReplace dental implants because the cap label incorrectly lists measurements as 5.0x8mm instead of the actual 4.3x10mm.

    Product
    NobelReplace Conical Connection (CC) PMC RP 4.3x10mm, REF: 37291 - Product Usage: implants are intended to be used in the upper or lower jaw bone (osseointegration) and used for anchoring or supporting tooth replacements to restore chewing function.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2805-2020·2020-08-26

    PVA PREVENT Emergency Ventilator Recalled for Potential Incomplete Air Delivery

    Precision Valve & Automation is recalling three PVA PREVENT emergency ventilators due to a software error that may cause false alarms or incomplete air delivery cycles.

    Product
    PVA, PREVENT is an FDA-authorized emergency ventilator designed to treat patients suffering from COVID-19 respiratory failure. This motorized device automatically compresses a resuscitator bag to provide air to the lungs of a COVID-19 patient, eliminating the human error and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V505000·2020-08-26

    2020 Audi SQ5 and Volkswagen vehicles recalled for defective seat welds

    Certain 2020 Audi SQ5 and Q5 vehicles and 2020-2021 Volkswagen models have improperly welded front seat frames. In a rear-end crash, the defective welds could fail and reduce occupant restraint, increasing the risk of injury.

    Product
    AUDI — AUDI, VOLKSWAGEN Q5, SQ5, ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2816-2020·2020-08-26

    DePuy Synthes LCP Plate Recall Due to Dimensional Tolerance Issues

    Synthes (USA) Products LLC is recalling 191 units of DePuy Synthes Trauma LCP One-Third Tubular Plates because dimensional features may be out of tolerance, potentially reducing locking strength.

    Product
    DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Holes / 93mm - Product Usage: intended for fixation of fractures, osteotomies and non-unions of clavicle, scapula, olecranon, humerus, radius, ulna, pelvis, distal tibia and fibula, particularly in osteopenic bone.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2807-2020·2020-08-26

    Chembio DPP COVID-19 IgM/IgG System Recalled for Performance Issues

    Chembio Diagnostics is recalling 7,674 kits of the DPP COVID-19 IgM/IgG System because the FDA revoked its Emergency Use Authorization due to performance issues.

    Product
    Chembio DPP COVID-19 IgM/IgG System- Rrapid immunochromatographic test for the qualitative detection and differentiation of Immunoglobulin M (IgM) and Immunoglobulin G (IgG) antibodies to SARS-CoV-2 in fingerstick whole blood, venous whole blood, serum, or plasma (lithium…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2818-2020·2020-08-26

    Smith & Nephew Recalls Single RIKKI Retractors Due to Improper Heat Treatment

    Smith & Nephew is recalling 111 units of Single RIKKI Retractors because they were improperly heat treated. The devices are used during surgery to hold soft tissue away from the surgical site.

    Product
    Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the surgical site.
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Drugs)·D-1508-2020·2020-08-26

    Lannett Recalls Prednisone Tablets Due to Labeling Error

    Lannett Company, Inc. is recalling specific batches of Prednisone Tablets due to a labeling error where 2.5 mg bottles contained 10 mg tablets.

    Product
    Prednisone Tablets, USP 2.5 mg, 100 tablets, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, Manufactured by: Tianjin Tianyao Pharmaceuticals Co., Ltd No. 221 Huanghai Road, Tianjin Economical-Technological Development Area, Tianjin, China 300457 NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2806-2020·2020-08-26

    Argon Medical Devices Recalls ClosureFast Micro Introducer Sheath Sets

    Argon Medical Devices is recalling 1,000 units of ClosureFast Micro Introducer Sheath Sets because the sterile products were manufactured under one lot with different expiration dates.

    Product
    ClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage: Introducer Products are stand-alone components, standard kits, or convenience kits built to user specifications. These products facilitate access to a vein or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1526-2020·2020-08-26

    Calvin Scott Recalls Phentermine HCL Capsules Due to Packaging Defects

    Calvin Scott & Company is recalling specific lots of Phentermine HCL capsules because light-sensitive products were repackaged in transparent pouches.

    Product
    Phentermine HCL GrayYellow capsules, 15mg, packaged in a) 28-count bags and b) 56-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: Tagi Pharma, South Beloit, IL 61080; NDC 51224-0203-70
    Category
    Drug
    Distribution
    Distributed nationwide