The Recall Desk

State

Tennessee product recalls

73,809 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,860
Critical
1,324
Severe
1,974
Most recent
2026-11-04

Of the 7,860 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 1,974 (25%) are Severe.

These figures cover only the 7,860 recalls whose distribution notice names Tennessee specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39851–39875 of 81669

  • HighNHTSA·18V827000·2018-11-22

    New Flyer Bus Recall for Fire Extinguisher Actuator Defect

    New Flyer is recalling certain 2013-2017 buses because a fire extinguisher actuator may fail, preventing the suppression system from discharging during a fire.

    Product
    NEW FLYER — NEW FLYER XN60, XN40, XD40, XDE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0616-2019·2018-11-21

    Ukrop's Roasted Turkey and Colby Jack Sub Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling Roasted Turkey & Colby Jack Subs because they may have contacted equipment used to process country ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Roasted Turkey & Colby Jack Sub, NET WT 8.3 OZ (235g), UPC 72251525142
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-0288-2019·2018-11-21

    Euphoric Male Performance Enhancer Recalled for Undeclared Prescription Drugs

    Epic Products, LLC is recalling Euphoric Premium Male Performance Enhancer capsules because they contain undeclared sildenafil, tadalafil, and oxytetracycline.

    Product
    Euphoric Premium Male Performance Enhancer capsules, packaged in a)1-count blister cards, UPC 6 96859 28646 9, b) 3-count bottle, UPC 6 96859 28647 6 and c) 12-count bottle, UPC 6 96859 28648 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0610-2019·2018-11-21

    Ukrop's Ham on Petite Party Rolls Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling 44 packages of Ham on Petite Party Rolls because they may have contacted equipment used to process country ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Ham on Petite Party Rolls 20CT, NET WT 21.8 OZ (1.36lb/618g) , UPC 72251524094
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0609-2019·2018-11-21

    Ukrop's Cuban Style Sub Recalled for Listeria Equipment Contact

    Ukrop's Homestyle Foods is recalling 2,600 packages of Cuban Style Subs because they may have contacted equipment used to process country ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Cuban Style Sub, NET WT 8.3 OZ (235g), UPC 72251525152
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0605-2019·2018-11-21

    Ukrop's Black Forest Ham and Provolone Sub Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling 2,702 packages of Black Forest Ham & Provolone Subs because they may have contacted equipment used to process ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Black Forest Ham & Provolone Sub NET WT 7.8 OZ (221g) UPC 72251525153
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0607-2019·2018-11-21

    Ukrop's Country Ham Rolls Recalled for Listeria Contact Risk

    Ukrop's Homestyle Foods is recalling 35 packages of Country Ham on Petite Party Rolls because they may have contacted equipment used for ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Country Ham on Petite Party Rolls 20CT, NET WT 17.7 OZ (1.11lb/502g), UPC 72251524487
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0608-2019·2018-11-21

    Ukrop's Country Ham Sandwiches Recalled for Listeria Equipment Contact

    Ukrop's Homestyle Foods is recalling Country Ham on White House Rolls because they may have contacted equipment used to process ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Country Ham on White House Rolls 12CT, 2CT, 6CT, NET WT 23.3 OZ (1.46lb/660g), NET WT 3.9 OZ (110g), NET WT 11.6 OZ (330g), UPC 72251524485, 72251524479,72251524486
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0612-2019·2018-11-21

    Ukrop's Honey Ham and Swiss Rolls Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling Honey Ham & Swiss on White House Rolls because they may have contacted equipment used to process country ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Honey Ham & Swiss on White House Rolls 2CT, NET WT 5.5 OZ (155g) UPC 72251525075
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0606-2019·2018-11-21

    Ukrop's Country Ham on Petite Biscuits Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling 88 packages of Country Ham on Petite Biscuits because they may have contacted equipment used for ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Country Ham on Petite Biscuits 8CT, NET WT 14 OZ (397g), UPC 72251524271
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0615-2019·2018-11-21

    Ukrop's Italian Style Sub Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling Italian Style Subs because they may have contacted equipment used for recalled country ham containing Listeria monocytogenes.

    Product
    Ukrop's Italian Style Sub , NET WT 8.2 OZ (232g) UPC 72251525151
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0261-2019·2018-11-21

    Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination

    Sandoz Inc. is recalling 1,550 bottles of Isosorbide Dinitrate Tablets 20 mg due to cross-contamination with other products.

    Product
    Isosorbide Dinitrate Tablets, USP 20 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-222-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0246-2019·2018-11-21

    Zero Xtreme Dietary Supplement Recalled for Undeclared Sibutramine

    Zero Xtreme USA is recalling 16 bottles of Zero Xtreme Dietary Supplement capsules because they contain undeclared sibutramine and were marketed without an approved NDA or ANDA.

    Product
    Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro Sanitario No SD2014-0002208 LLC-USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0370-2019·2018-11-21

    GE Healthcare Recalls Gamma Camera Systems Due to Falling Detector Risk

    GE Healthcare is recalling 1,166 Millennium MG gamma camera systems because a detector can detach and fall.

    Product
    GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma Camera H3000ZL Acquisition System
    Category
    Medical Device
    Distribution
    50 states
  • SevereFDA (Devices)·Z-0448-2019·2018-11-21

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus Hip Fracture Nail Left 125 Deg 11x300mm, Item Number 814411300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0413-2019·2018-11-21

    GE Healthcare Recalls Aisys Anesthesia System Touchscreen Display Kits

    GE Healthcare is recalling 4,207 Aisys anesthesia system touchscreen display kits because they fail to transition to backup ventilation if a patient stops breathing.

    Product
    Touchscreen display kit. Sold under the following product names: TOUCHSCREEN DISPLAY KIT 11.X ENGLISH FOR USA, TOUCHSCREEN DISPLAY KIT 11.X ENGLISH, TOUCHSCREEN DISPLAY KIT 11.X GERMAN, TOUCHSCREEN DISPLAY KIT 11.X DUTCH, TOUCHSCREEN DISPLAY KIT 11.X FRENCH, TOUCHSCREEN…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V826000·2018-11-21

    Navistar Recalls 2018-2019 International Trucks for Clutch Assembly Defect

    Navistar is recalling certain 2018-2019 International trucks because a clutch component may fail, causing unintended vehicle movement and increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL RH, MV, LONESTAR, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0259-2019·2018-11-21

    Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination

    Sandoz Inc. is recalling Isosorbide Dinitrate Tablets 5 mg due to cross-contamination with other products. The recall affects 7,817 bottles distributed nationwide.

    Product
    Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0260-2019·2018-11-21

    Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination

    Sandoz Inc. is recalling 5,100 bottles of Isosorbide Dinitrate Tablets, USP 10 mg, due to cross contamination with other products.

    Product
    Isosorbide Dinitrate Tablets, USP 10 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-225-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0276-2019·2018-11-21

    Taro Recalls Children's Allergy Solution Due to Impurity

    Taro Pharmaceuticals is recalling 12,432 bottles of Children's 24 Hour Allergy Oral Solution because an unknown impurity exceeded limits during stability testing.

    Product
    Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL, Bubble Gum Flavor, Sugar Free/Dye Free, 4 FL OZ (120 mL) bottle, Dist. by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0250-2019·2018-11-21

    Kadesh Recalls Puriton Eye Relief Drops for Non-Sterility

    Kadesh International is recalling Puriton Eye Relief Drops because they were manufactured under non-sterile production conditions.

    Product
    puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0614-2019·2018-11-21

    Ukrop's Honey Turkey and Cheddar Rolls Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling Honey Turkey & Cheddar on White House Rolls because they may have contacted equipment used to process country ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Honey Turkey & Cheddar on White House Rolls 2CT, NET WT 5.5 OZ (155g), UPC 72251525074
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0611-2019·2018-11-21

    Ukrop's Ham on White House Rolls Recalled for Listeria Risk

    Ukrop's Homestyle Foods is recalling 67 packages of Ham on White House Rolls because they may have contacted equipment used to process country ham recalled for Listeria monocytogenes.

    Product
    Ukrop's Ham on White House Rolls 12CT, NET WT 26.9 OZ (1.68lb/762g) UPC 72251525154 ,
    Category
    Food
    Distribution
    5 states