The Recall Desk

State

Tennessee product recalls

73,833 recalls have nationwide distribution and so reach Tennessee. 7,861 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,861
Critical
1,324
Severe
1,974
Most recent
2026-11-14

Of the 7,861 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 7,861 recalls whose distribution notice names Tennessee specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55101–55125 of 81694

  • ModerateFDA (Devices)·Z-1189-2016·2016-03-30

    Zimmer Spine Universal Clamp System Recall for Updated Cleaning Instructions

    Zimmer Spine is issuing a correction notice for the Universal Clamp System to provide updated cleaning and disinfecting instructions.

    Product
    Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and helps reduce spinal deformities and fractures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0781-2016·2016-03-30

    AstraZeneca Recalls Tudorza Pressair Inhalers Due to Defective Delivery System

    AstraZeneca is recalling Tudorza Pressair inhalers because some units have actuation counters set to a number other than 60.

    Product
    Tudorza Pressair (aclindinium bromide inhalation powder), 400 mcg per actuation, 60 Metered Doses per Inhaler, Rx Only. Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850. Manufactured by: Forest Laboratories, Ireland Limited, Dublin 17 Ireland. Product of…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1233-2016·2016-03-30

    Roche cobas p 512 Pre-analytical System Recalled for Sample Spillage

    Roche is recalling 35 cobas p 512 pre-analytical systems because a sensor defect causes open sample tubes to drop and spill.

    Product
    cobas p 512 pre-analytical system Pre-analytical sample handling that includes de-capping, aliquoting and sorting of samples for analysis.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1232-2016·2016-03-30

    Siemens syngo X Workplace Medical Workstation Recalled for Segmentation Error

    Siemens Medical Solutions USA is recalling six syngo X Workplace medical workstations because imported segmentation results appear mirrored, rendering them unusable for ablation procedures.

    Product
    syngo X Workplace is a medical workstation for real-time viewing, image manipulation, 3D-visualization, communication, and storage of medical images and data on exchange media. It is used for diagnostic image viewing and post processing during interventional procedures. .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1240-2016·2016-03-30

    Siemens Estradiol Test Recalled Due to Potential False Results

    Siemens is recalling ADVIA Centaur Enhance Estradiol tests because the drug fulvestrant may cause falsely elevated results.

    Product
    Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number: 10490889, 10491445, 10697757 Product Usage: For in vitro diagnostic use in the quantitative determination of estradiol in human serum and plasma (heparinized and EDTA) using the ADVIA Centaur¿, ADVIA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1190-2016·2016-03-30

    Zimmer Biomet Issues Correction Notice for Instinct Java System Cleaning Instructions

    Zimmer Biomet is issuing a correction notice to provide updated cleaning and disinfecting instructions for the Instinct Java System and Universal Clamp System.

    Product
    Instinct¿ Java¿ System (IFU reference: 046WAN0000T) . Stabilizes one or more vertebral segments from the thoracic spine to the sacrum during the development of bone tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1247-2016·2016-03-30

    Neurotherm Curved Radiofrequency Cannula Recalled for Mislabeling

    Neurotherm, Inc. is recalling 135 curved radiofrequency cannulas because straight needles were incorrectly labeled as curved.

    Product
    Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18 Product Usage: The device is a radiofrequency needle, used for the application of radiofrequency energy with as intended result, thermo coagulation of nervous tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V176000·2016-03-29

    Forest River Georgetown RVs Recalled for Missing Emergency Egress Window

    Forest River is recalling 2015-2017 Georgetown RVs because a vented window was installed instead of a required secondary egress window, posing a risk of entrapment.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V175000·2016-03-29

    Forest River Recalls 2013-2016 Puma Trailers for Tire Clearance Issue

    Forest River is recalling 2013-2016 Puma recreational trailers because tires may contact the wheel well on bumps, risking tire damage and loss of control.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V177000·2016-03-29

    Terex Recalls 2011-2016 Aerial Devices Due to Inadequate Boom Tip Welds

    Terex is recalling 2011-2016 aerial devices because inadequate welds at the boom tip may cause the platform to tilt unexpectedly, increasing the risk of user injury.

    Product
    TEREX — TEREX AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16124·2016-03-28

    Fiskars 32-Inch Bypass Lopper Shears Recalled for Laceration Hazard

    CPSC reannounced the recall of Fiskars 32-inch bypass lopper shears after additional injuries were reported. Consumers should stop using the product and contact Fiskars for a free replacement.

    Product
    Fiskars® 32-Inch Bypass Lopper Shears
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V173000·2016-03-25

    BMW Recalls 2016 7 Series Vehicles Due to Air Bag Control Module Defect

    BMW is recalling 6,110 model year 2016 740Li, 750Li, and 750Lxi vehicles because the air bag control module may reset, preventing air bags from deploying in a crash.

    Product
    BMW — BMW 750LXI, 740LI, 750LI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V171000·2016-03-24

    Volkswagen Recalls 2012-2014 Passat TDI Vehicles for Fire Risk

    Volkswagen is recalling 2012-2014 Passat TDI vehicles because water can corrode electrical connectors, causing a short that may lead to a fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E023000·2016-03-24

    Honda Recalls PCX Scooter Accessory Trunk Bases for Detachment Risk

    Honda is recalling accessory rear trunk bases for PCX125 and PCX150 scooters because the locking hook may not fully engage, allowing the trunk to detach while riding.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0772-2016·2016-03-23

    Wilderness Family Naturals Recalls Butternut Squash Soup for Milk Contamination

    Wilderness Family Naturals is recalling specific lots of Butternut Squash Soup due to potential milk contamination from an ingredient.

    Product
    Morning Star Disaster Supplies Butternut Squash Soup, Net Wt 4.75oz (135 g). UPC 853328-006113, Foil Bag Wilderness Family Naturals Quick Meal Butternut Squash Soup, Net Wt 4.75 oz (135 g). UPC 853328-006182, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0766-2016·2016-03-23

    Wilderness Family Naturals Tomato Basil Soup Recalled for Milk Contamination

    Wilderness Family Naturals is recalling specific Tomato Basil Soup products due to potential milk contamination. The recall covers over 5,500 units distributed in the US and Canada.

    Product
    Morning Star Disaster Supplies Tomato Basil Soup, Net Wt 3.88 oz (110 g), UPC 853328-006120, Foil Bag Wilderness Family Naturals Quick Meal Tomato Basil Soup, Net Wt 3.88 oz (110 g). UPC 853328-006243, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0760-2016·2016-03-23

    Wilderness Family Naturals Coconut Chia Pudding Mix Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Chia Pudding Mix due to potential milk contamination. The product was distributed nationwide in the US and in Canada.

    Product
    Wilderness Family Naturals Coconut Chia Pudding Mix Sweetened with Coconut Sap Sugar Organic Packaged in the following sizes: 1.1 lb. Plastic Bag, UPC 898392-007796 and 13.2 lb. (12 Plastic Bags in a cardboard box), UPC 01002467
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0774-2016·2016-03-23

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling Paricalcitol Capsules because stability testing revealed out-of-specification impurities. The recall covers 30,891 bottles distributed nationwide and in Puerto Rico.

    Product
    Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By: Pharmaceutics International, Inc., Hunt Valley, MD 21031, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-7656-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0765-2016·2016-03-23

    Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and specific chowder products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies ,Creamy Potato Corn Chowder, Net Wt. 7.88 oz (223 g). UPC 853328-006052, Foil Bag Wilderness Family Naturals Quick Meal Potato Corn Chowder, Net Wt 7.88 oz (223 g). UPC 853328-006199, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0767-2016·2016-03-23

    Wilderness Family Naturals Coconut Milk Powder Recalled for Milk Contamination

    Wilderness Family Naturals is recalling Organic Coconut Milk Powder and related products due to potential milk contamination.

    Product
    Morning Star Disaster Supplies Creamy Coconut Rice Soup, Net Wt 7.25 oz (206 g). UPC 853328-006038, Foil Bag Wilderness Family Naturals Quick Meal Creamy Coconut Rice Soup, Net Wt 7.25 oz (206 g). UPC 853328-006038, Foil Bag
    Category
    Food
    Distribution
    Distributed nationwide