The Recall Desk

State

Tennessee product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52301–52325 of 81688

  • CriticalFDA (Food)·F-1924-2016·2016-08-24

    Greenland Trading Recalls Al Rasheed Sardines Due to Botulism Risk

    Greenland Trading Corp is recalling Al Rasheed Sardines due to potential C. botulinum contamination. The product was distributed in seven states.

    Product
    Al Rasheed Sardine Item #4017 Label not available - NYSDAM sampling.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1942-2016·2016-08-24

    Oregon Potato Company Recalls Frozen White Onion Dice for Listeria Risk

    Oregon Potato Company is voluntarily recalling IQF 1/4" Frozen White Onion Dice due to potential Listeria monocytogenes contamination.

    Product
    IQF 1/4" Frozen WHITE Onion Dice, item number 103342, bulk cases, net wt. 45 lbs.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1938-2016·2016-08-24

    Oregon Potato Company Recalls Frozen Yellow Onion Dice for Listeria Risk

    Oregon Potato Company is voluntarily recalling specific lots of frozen yellow onion dice due to potential Listeria monocytogenes contamination.

    Product
    IQF 1/4" Yellow Onion Dice, frozen, item numbers: 103364, 103381, and 104831, bulk cases, net wt. 45 lbs.; 11244CH Onion Dice 1/4, frozen, item number 103381, bulk cases, net wt. 45 lbs. Onion, Diced 1/4" IQF 45#CS, item number 104155, bulk cases, net wt. 45 lbs.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1943-2016·2016-08-24

    Oregon Potato Company Recalls Fresh White Onion Dice for Listeria Risk

    Oregon Potato Company is voluntarily recalling fresh white onion dice due to potential Listeria monocytogenes contamination. The product was distributed across multiple US states, Canada, and Ireland.

    Product
    3/8" White Onion Dice- FRESH, item number 105197, bulk tote, net wt. 1250 lbs.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1946-2016·2016-08-24

    Oregon Potato Company Recalls Frozen Yellow Onion Dice for Listeria Risk

    Oregon Potato Company is voluntarily recalling 3/8" Frozen Yellow Onion Dice due to potential Listeria monocytogenes contamination. The product was distributed in 17 US states, Canada, and Ireland.

    Product
    705000 IQF 3/8" Dice Yellow Onion, item number 101472, bulk tote, net wt. 1250 lbs. IQF 3/8" Yellow Onion Dice, item number 103330, 103341, bulk cases, net wt. 20 lbs. IQF 3/8" Yellow Onion Dice, item numbers 101578, 104147, and 104193, bulk cases, net wt. 45 lbs. IQF…
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1941-2016·2016-08-24

    Oregon Potato Company Recalls Frozen Yellow Onion Dice for Listeria Risk

    Oregon Potato Company is voluntarily recalling IQF 3/4" Yellow Onion Dice due to potential Listeria monocytogenes contamination.

    Product
    IQF 3/4" Yellow Onion Dice, Frozen, item number 101430, bulk tote, net wt. 1200 lbs.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Drugs)·D-1458-2016·2016-08-24

    Golden State Medical Supply Recalls Venlafaxine Hydrochloride Extended-Release Capsules

    Golden State Medical Supply Inc. is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, due to failed dissolution specifications.

    Product
    Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-123-90, Rx Only, GSMS.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2567-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recalled for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Flat L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 119,770 units distributed worldwide.

    Product
    Valleylab Laparoscopic Flat L-Hook Electrode 36CM Item Code: E277436 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction via a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1940-2016·2016-08-24

    Oregon Potato Company Recalls Frozen Yellow Onion Dice for Listeria Risk

    Oregon Potato Company is voluntarily recalling IQF 3/8" Un-Blanched Yellow Onion Dice due to potential Listeria monocytogenes contamination.

    Product
    IQF 3/8" Un-Blanched Yellow Onion Dice, Frozen, item number 103349, bulk cases, net wt. 45 lbs.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1922-2016·2016-08-24

    Newly Weds Foods Recalls Flour Breader Contaminated with E. coli O121

    Newly Weds Foods Inc is recalling bulk flour bland breader contaminated with E. coli O121. The product was distributed nationwide in 15, 30, and 50 lb bags or boxes.

    Product
    Bulk flour bland breader packaged into 15, 30, and 50 lb bags or boxes.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2575-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recall for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Wire L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 50,055 units distributed worldwide.

    Product
    Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code: E2783R36ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1932-2016·2016-08-24

    HelloFresh Recalls Summer Vegetable Salad Due to Listeria Risk

    HelloFresh is recalling Summer Vegetable Salad with Seared Chicken due to possible Listeria monocytogenes contamination. The product was distributed in 28 states.

    Product
    Summer Vegetable Salad with Seared Chicken, Garlic Croutons, and Mustard-Chive Vinaigrette
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Food)·F-1939-2016·2016-08-24

    Oregon Potato Company Recalls Frozen Yellow Onion Strips for Listeria Risk

    Oregon Potato Company is voluntarily recalling specific lots of frozen yellow onion strips due to potential Listeria monocytogenes contamination.

    Product
    IQF 3/8" Yellow Onion Strip, Frozen, Item number 103331, bulk tote, net wt. 1150 lbs. IQF 3/8" Yellow Onion Strip, Frozen, item number 103368, bulk case, net wt. 40 lbs. Onion, Strips 3/8" 103369 40#, item number 103369, bulk case, net wt. 40 lbs. IQF 3/8" Yellow…
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1944-2016·2016-08-24

    Oregon Potato Company Recalls Fresh White Onion Strips for Listeria Risk

    Oregon Potato Company is voluntarily recalling fresh white onion strips due to potential Listeria monocytogenes contamination.

    Product
    3/8" White Onion Strip-FRESH, item number 105196, bulk totes, net wt. 1200 lbs.
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-2577-2016·2016-08-24

    Medtronic Recalls Laparoscopic Electrode Due to Sterile Barrier Compromise Risk

    Medtronic is recalling 3,470 Valleylab Laparoscopic Flat L-Hook Electrodes because the package may be compromised, potentially breaching the sterile barrier.

    Product
    Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code: E2784R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2572-2016·2016-08-24

    Medtronic Recalls Laparoscopic Electrodes Due to Sterile Barrier Compromise

    Medtronic is recalling 1,440 Valleylab Laparoscopic Wire J-Hook Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.

    Product
    Valleylab Laparoscopic Wire J-Hook Electrode Retractable 28CM Item Code: E2782R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2582-2016·2016-08-24

    Synthes Recalls Titanium Single Vector Distractor Bodies Due to Fastener Separation Risk

    Synthes (USA) Products LLC is voluntarily recalling 182 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.

    Product
    TI Single Vector Distractor Body with Left Foot/20mm; Catalog ID 487.963 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2581-2016·2016-08-24

    Synthes Recalls Titanium Single Vector Distractor Bodies Due to Fastener Separation Risk

    Synthes (USA) Products LLC is voluntarily recalling 90 units of Titanium Single Vector Distractor Bodies because the fastener may separate prematurely from the Proximal Foot Plate.

    Product
    TI Single Vector Distractor Body with Right Foot/20mm; Catalog ID 487.962 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for mandibular bone lengthening where gradual bone distraction is required, including conditions such as congenital mandibular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V615000·2016-08-24

    Hyundai Recalls 2016 Sonata Vehicles Due to Driver Air Bag Defect

    Hyundai is recalling specific 2016 Sonata vehicles because the driver-side frontal air bag may not adequately protect the driver's neck in a crash.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2555-2016·2016-08-24

    Medtronic Recalls Valleylab Laparoscopic Argon Electrodes Due to Sterile Barrier Risk

    Medtronic is recalling 19,200 Valleylab Laparoscopic Flexible Argon Electrodes because the packaging may be compromised, potentially breaching the sterile barrier.

    Product
    Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code: E25303 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2423-2016·2016-08-24

    Biomet 3i Recalls Dental Implants Due to Potential Unsealed Pouches

    Biomet 3i is recalling 1,648,273 dental implants because pouches may not have been sealed during packing, potentially compromising sterility.

    Product
    LDA Screw SBL 4mm(D) Item: SCRSBL2 Dental implants
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2558-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recall for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Argon Modified Flat l Electrodes due to a potential sterile barrier breach.

    Product
    Valleylab Laparoscopic Argon Modified Flat l Electrode 28CM Item Code: E258128 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2574-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recall for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Wire L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 63,320 units distributed worldwide.

    Product
    Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code: E2783R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2570-2016·2016-08-24

    Medtronic Valleylab Laparoscopic Electrode Recall for Sterile Barrier Compromise

    Medtronic is recalling Valleylab Laparoscopic Curved Spatula Electrodes due to a potential sterile barrier breach. The recall covers lots 209358X through 60870083X distributed worldwide.

    Product
    Valleylab Laparoscopic Curved Spatula Electrode Retractable 28CM Item Code: E2781R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2541-2016·2016-08-24

    TYRX Neuro Absorbable Antibacterial Envelope Recalled for Manufacturing Validation Issues

    TYRX Inc. is recalling 194 units of the TRYX Neuro Absorbable Antibacterial Envelope because manufacturing processes were not adequately validated.

    Product
    TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
    Category
    Medical Device
    Distribution
    Distributed nationwide