The Recall Desk

State

Tennessee product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31301–31325 of 81597

  • ModerateFDA (Devices)·Z-2533-2020·2020-07-15

    Teleflex Recalls RUSCH LASERTUBE Devices Due to Laser Guard Foil Separation

    Teleflex is voluntarily recalling 6,014 RUSCH LASERTUBE devices because the laser guard foil may partially separate or detach at the edges when exposed to moisture.

    Product
    RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 102004-000050 c) I.D. mm 6,0, Product Code 102004-000060 d) I.D. mm 7,0, Product Code 102004-000070 e) I.D. mm 8,0, Product Code 102004-000080 Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1374-2020·2020-07-15

    Somerset Therapeutics Recalls Brimonidine Tartrate Ophthalmic Solution

    Somerset Therapeutics is recalling Brimonidine Tartrate Ophthalmic Solution 0.2% due to a slow leaching process from the product label that may impact the product over its shelf life.

    Product
    BRIMONIDINE TARTRATE — BRIMONIDINE TARTRATE (BRIMONIDINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1375-2020·2020-07-15

    Somerset Therapeutics Recalls Brimonidine Tartrate Ophthalmic Solution

    Somerset Therapeutics is recalling Brimonidine Tartrate Ophthalmic Solution 0.2% due to a slow leaching process from the product label that may impact the product over its shelf life.

    Product
    BRIMONIDINE TARTRATE — BRIMONIDINE TARTRATE (BRIMONIDINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V406000·2020-07-14

    Setra Motorcoaches Recalled for Electronic Stability Control Defect

    Daimler Coaches North America is recalling 2018-2020 Setra motorcoaches because the Electronic Stability Control system can be disabled at unsafe speeds, increasing crash risk.

    Product
    SETRA — SETRA S417 TC, S407 CC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V405000·2020-07-14

    Jayco Recalls 2016-2018 Motorhomes Due to Leveling System Bracket Failure

    Jayco is recalling specific 2016-2018 motorhomes because a mounting bracket for the leveling system may fail, allowing components to contact the ground and increasing crash risk.

    Product
    JAYCO — JAYCO GREYHAWK, REDHAWK, ENVOY 200, ENVOY 100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E048000·2020-07-13

    Curt Rambler RV Towbars Recalled for Axial Pivot Pin Failure Risk

    Curt Manufacturing is recalling Rambler RV Towbars because the axial pivot pin may loosen or fail, potentially causing the hitch to separate and increasing crash risk.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V403000·2020-07-13

    Mitsubishi Outlander Recall: Second-Row Seat Belt Buckle Interference

    Mitsubishi is recalling 2014-2019 Outlander and 2018-2019 Outlander PHEV vehicles because the second-row center seat belt buckle may interfere with the right-side buckle, rendering it inoperable.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER PHEV, OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V400000·2020-07-10

    Forest River Recalls 2021 Riverstone Trailers Due to Wiring Defect

    Forest River is recalling specific 2021 Riverstone trailers equipped with an optional generator prep package due to incorrect transfer switch wiring that may cause voltage back feed.

    Product
    FOREST RIVER — FOREST RIVER RIVERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20761·2020-07-09

    RH Recalls Riveted Mesh Floor Lamps Due to Fire Hazard

    RH is recalling Riveted Mesh Floor Lamps because the foot switch can overheat or catch fire. Consumers should stop using the lamps and contact RH for a refund.

    Product
    Riveted Mesh Floor Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20759·2020-07-09

    Ananda Apothecary Recalls Essential Oils Due to Non-Child-Resistant Packaging

    Ananda Apothecary is recalling four essential oil products because their packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.

    Product
    Wintergreen 100% Pure Essential Oil, Sweet Birch 100% Pure Essential Oil, Super Soother Pure Essential Oil Blend, and Breathe Deep Pure Essential Oil Blend
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1027-2020·2020-07-08

    Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert Recalled for Undeclared Milk

    Beyond Better Foods is recalling Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert because it may contain undeclared milk.

    Product
    Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert, one Pint (473 ml). Case GTIN: 1-08-52109-33106-9. Item UPC:8-52109-33150-5. Produced exclusively for: Beyond Better Foods, LLC, Bronx, NY
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1015-2020·2020-07-08

    Mount Franklin Foods Recalls 7-Select Yogurt Pretzels for Undeclared Peanuts

    Mount Franklin Foods is recalling 7-Select Yogurt Pretzels because they may contain undeclared peanuts. The product was distributed to 7-11 stores nationwide.

    Product
    7-Select Yogurt Pretzels Naturally Flavored Vanilla Crunchy Pretzel Covered in a Vanilla Yogurt NET WT 5 OZ (142 g) UPC 5254856657
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2439-2020·2020-07-08

    LivaNova SCP Pump Control Panel Recalled for Rotary Knob Wear

    LivaNova is recalling eight SCP Pump Control Panels because premature wear of the angle encoder may make the rotary knob difficult or impossible to rotate during cardiopulmonary bypass.

    Product
    Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF 60-02-50, IPX2, RxOnly, UDI: 04033817900993
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Drugs)·D-1359-2020·2020-07-08

    Koala Hand Sanitizer Recalled for Subpotent Ethanol and Undeclared Isopropyl Alcohol

    Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol content is below the label claim and undeclared isopropyl alcohol is present.

    Product
    Koala Hand Sanitizer, Unscented, 16 FL OZ., Antibacterial, (Ethyl Alcohol 70%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2440-2020·2020-07-08

    LivaNova SCP Pump Control Panel Recalled Due to Rotary Knob Wear

    LivaNova is recalling 24 SCP Pump Control Panels because the rotary knob may fail to rotate due to premature wear, risking patient injury during surgery.

    Product
    Control Panel REF - 60-02-15: LivaNova SCP Pump Control Panel. REF 60-02-15, IPX2, RxOnly, UDI: 04033817900986
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Devices)·Z-2463-2020·2020-07-08

    LivaNova Recalls Vein Irrigation Cannulas Due to Sterile Barrier Breach

    LivaNova USA Inc. is recalling 150 units of Vein Irrigation Cannulas with blunt tips because internal tests identified potential breaches in the sterile barrier.

    Product
    Vein Irrigation Cannula with blunt tip. ASY BIC, STERILE 25/CS REF/ GTIN for Insert Label:BIC/ 00803622133091
    Category
    Medical Device
    Distribution
    44 states
  • SevereFDA (Drugs)·D-1357-2020·2020-07-08

    Koala Hand Sanitizer Recalled for Subpotent Alcohol and Undeclared Ingredients

    Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol level is below the label claim and it contains undeclared isopropyl alcohol.

    Product
    Koala Hand Sanitizer, Soothing Eucalyptus, 16 FL OZ., Antibacterial, (Ethyl Alcohol 68%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1360-2020·2020-07-08

    Metformin Hydrochloride Extended-Release Tablets Recalled for NDMA Impurity

    The Harvard Drug Group is recalling Metformin Hydrochloride Extended-Release Tablets due to potential NDMA impurity levels above established limits.

    Product
    Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 100 Tablets (10 x 10) unit dose cartons, Rx only, Manufactured by: Apotex, Inc., Toronto, Ontario, Canada, Manufactured for: Apotex Corp. Weston, FL, Distributed by: Major Pharmaceuticals, Livonia, MI 48152 NDC…
    Category
    Drug
    Distribution
    Distributed nationwide