The Recall Desk

State

Tennessee product recalls

73,092 recalls have nationwide distribution and so reach Tennessee. 7,851 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,327
Severe
1,665
Most recent
2026-09-23

Of the 7,851 recalls naming Tennessee we have scored against our rubric, 1,327 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,665 (21%) are Severe.

These figures cover only the 7,851 recalls whose distribution notice names Tennessee specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8101–8125 of 80943

  • HighCPSC·25146·2025-02-20

    Sauder Tip-Over Restraint Straps Recalled Due to Failure Risk

    Sauder is recalling about 15,800 tip-over restraint straps used on dressers and 4-drawer chests manufactured from July 2020 to August 2023. The straps can fail to prevent tip-over and entrapment hazards to children.

    Product
    Sauder and Sauder Beginnings Dressers and 4-Drawer Chests tip-over restraint straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25149·2025-02-20

    Super73 Electric Bicycles Recalled for Brake Failure and Crash Hazard

    Super73 is recalling about 1,400 Model Year 2024 Z Miami SE and Z Adventure Core e-bikes sold April-September 2024. A retaining pin in the disc brake calipers can dislodge, causing brake failure and crash/injury hazards.

    Product
    Model Year 2024 Z Miami SE and Z Adventure Core Electric Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25144·2025-02-20

    Triumph TF250-X Motorcycles Recalled for Electrical Short Circuits and Unintended Starting

    About 690 Triumph TF250-X motorcycles are recalled due to plastic switch cubes that crack when exposed to brake fluid, creating electrical short circuits that can cause the motorcycle to start unexpectedly. No injuries have been reported.

    Product
    Triumph TF250-X Closed Course Competition Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25147·2025-02-20

    Homebox Blackout Roller Window Shades recalled for strangulation and entanglement hazards

    Homebox Blackout Roller Window Shades sold on Amazon from December 2022 to September 2024 feature long operating cords that pose strangulation and entanglement hazards to children. Consumers should place cords up and away from children.

    Product
    Homebox Blackout Roller Window Shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V108000·2025-02-20

    Indian Recalls 2025 Motorcycles Due to Fuel Pump Wire Defect

    Indian Motorcycle is recalling 2025 models due to a wire defect that may cause the fuel pump to fail and the engine to stall.

    Product
    INDIAN — INDIAN PURSUIT, ROADMASTER ELITE, SPRINGFIELD DARK HORSE, CHALLENGER DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1117-2025·2025-02-19

    Wheelchair Power Assist Speed Control Dial Recalled for Loss of Control Risk

    Max Mobility Smart Drive MX2+ SpeedControl Dial wheelchairs are being recalled due to faulty circuit boards that may cause loss of device control, potentially resulting in injury to users.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1165-2025·2025-02-19

    Exactech AcuMatch XLE Hip Implant Liner Recall

    Exactech is recalling certain AcuMatch XLE hip implant liners due to a missing ethylene vinyl alcohol barrier layer. The missing barrier may affect the implant's performance.

    Product
    AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL 0¿ LNR G 28MM 140-32-27 AM EHXL 0¿ LNR G 32MM 140-32-28 AM EHXL 0¿ LNR H 32MM 140-28-29 AM EHXL 0¿ LNR J 28MM 140-32-29 AM EHXL 0¿ LNR J 32MM 140-36-29 AM EHXL 0¿ LNR J 36MM 140-32-30 AM EHXL 0¿ LNR K 32MM
    Category
    Medical Device
    Distribution
    22 states
  • SevereFDA (Food)·F-0549-2025·2025-02-19

    Shirakiku Curvee Puffs Corn Puff Snack Recalled for Undeclared Milk Allergen

    Wismettac Asian Foods, Inc. is recalling Shirakiku brand Curvee Puffs Corn Puff Snack due to undeclared milk on the label. Consumers with dairy allergies should not consume this product.

    Product
    Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK, Sea Salt & Umami Flavor, NET WT 2.46 oz (70 g); Rear panel:Best Before YYYY.MM.DD; Nutritional Facts: 2.5 servings per container; Distributed by Wismettac Asian Foods, Inc.; 13409 Orden Drive, Santa Fe Spring, CA 90670;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0548-2025·2025-02-19

    Shirakiku Curvee Puffs Corn Puff Snack Recalled for Undeclared Milk Allergen

    Wismettac Asian Foods is recalling Shirakiku brand Curvee Puffs Corn Puff Snack because the product contains undeclared milk allergen. The affected product was distributed nationwide to approximately 471 consignees.

    Product
    Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK, Curry Flavor, NET WT 2.46 oz (70 g); Rear panel:Best Before YYYY.MM.DD; Nutritional Facts: 2.5 servings per container; Distributed by Wismettac Asian Foods, Inc.; 13409 Orden Drive, Santa Fe Spring, CA 90670; Product of
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0550-2025·2025-02-19

    Shirakiku Curvee Puffs Corn Snack Recalled for Undeclared Milk Allergen

    Wismettac Asian Foods is recalling Shirakiku brand Curvee Puffs Corn Puff Snacks due to undeclared milk. The product poses a serious risk to consumers with milk allergies. All lots distributed nationwide are affected.

    Product
    Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK, Corn Potage Flavor, NET WT 2.46 oz (70 g); Rear panel:Best Before YYYY.MM.DD; Nutritional Facts: 2.5 servings per container; Distributed by Wismettac Asian Foods, Inc.; 13409 Orden Drive, Santa Fe Spring, CA 90670; Produ
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1116-2025·2025-02-19

    Wheelchair Speed Control Remote Recalled Due to Loss-of-Control Risk

    The Smart Drive MX2+ SpeedControl Dial remote is being recalled due to a faulty circuit board that could cause loss of control of the wheelchair power assist, potentially resulting in injury.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1071-2025·2025-02-19

    Olympus Guide Sheath Kits recalled for potential radiopaque tip detachment

    Olympus Single Use Guide Sheath Kits (models K-201 through K-204) are recalled because the radiopaque tip of the guide sheath may detach and fall into the patient during respiratory procedures.

    Product
    Olympus Single Use Guide Sheath Kits with the following product descriptions and model numbers: 1. Single Use Guide Sheath Kit K-201 2.0MM Channel Set: Guide Sheath, Biopsy Forceps, Cytology Brush; Model Number: K-201 2. Single Use Guide Sheath Kit K-202 2.0MM Channel Set:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1168-2025·2025-02-19

    MediHoney Gel Wound Dressing Recall: Potential Induction Seal Defect

    Integra LifeSciences is recalling MediHoney Gel Wound & Burn Dressing Gel (Model 31815) due to potential induction seal defects in the tube packaging. Approximately 12,166 units were distributed worldwide, including throughout the United States and Malaysia.

    Product
    Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/Catalog Number: 31815 Software Version: N/A Product Description: MediHoney¿ Gel with Active Leptospermum Honey is a moist dressing made of Active Leptospermum Honey in combination with gelling
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1129-2025·2025-02-19

    Cardinal Health Presource Surgical Kits Recalled for Endotoxin Contamination

    Cardinal Health Presource Kits may contain endotoxin-contaminated non-sterile surgical strips and patties. These kits are used in surgical procedures and have been distributed worldwide including the US, Canada, and Saudi Arabia. Affected facilities should verify lot numbers against the recall list.

    Product
    Cardinal Health Presource Kits: 1) KIT, CAROTID ENDARTERECTOMY, Catalog Number:PVV20110B; 2) KIT, CAROTID ENDARTERECTOMY, Catalog Number:PVV20110D 3) KIT,CAROTID ENDARTERECTOMY, Catalog Number:PVV2CA103 4) KIT,CAROTID ENDARTERECTOMY, Catalog Number:PVV2CA10T 5) KIT,CAROTID E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0545-2025·2025-02-19

    Holiday Sprinkles Chocolate Drizzled Granola Mini Bars Recall for Metal Contamination

    Riverside Natural Foods has recalled Holiday Sprinkles Chocolate Drizzled Granola Mini Bars nationwide because the product may contain metal pieces. Consumers should not consume these bars.

    Product
    1.Holiday Sprinkles Chocolate Drizzled Granola Mini Bars 10.5oz (25 bars) 2.Holiday Sprinkles Chocolate Drizzled Granola Mini Bars 0.42oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0544-2025·2025-02-19

    Riverside Chocolate Drizzled Cookie Crumble Granola Bars Recalled for Metal Contamination

    Riverside Natural Foods is recalling Chocolate Drizzled Cookie Crumble Granola Bars distributed nationwide due to potential metal contamination. Approximately 2.4 million cases are affected.

    Product
    1. Chocolate Drizzled Cookie Crumble Granola Bars 4.2oz (5 bars) 2. Chocolate Drizzled Cookie Crumble Granola Bars 25.5oz (30 bars) 3. Chocolate Drizzled Cookie Crumble Granola Bars 0.85oz 4. Chocolate Drizzled Granola Bars Variety Pack 25.5oz (30 bars)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1134-2025·2025-02-19

    Cardinal Health Presource Surgical Kits Recalled for Potential Endotoxin Contamination

    Cardinal Health Presource surgical kits containing non-sterile strips and patties may be contaminated with endotoxins, posing potential risk to patients during surgical procedures.

    Product
    Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 1, Catalog Number:CHIP99NC12; 2) CHI STD NEURO CRANI OPT 1, Catalog Number:CHIP99NC13 3) CHI STD NEURO CRANI OPT 1, Catalog Number:CHIP99NC14 4) CHI STD NEURO CRANI OPT 1, Catalog Number:CHIP99NC15 5) CHI STD NEURO CRANI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1136-2025·2025-02-19

    Cardinal Health Presource Surgical Kits Recalled for Potential Endotoxin Contamination

    Cardinal Health is recalling Presource Kits (surgical strips and patties used in ophthalmic procedures) due to potential endotoxin contamination in non-sterile components.

    Product
    Cardinal Health Presource Kits: 1) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVA; 2) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVB 3) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVC 4) OCULAR PLASTIC PACK, Catalog Number:SEY35OP961 5) OCULAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1100-2025·2025-02-19

    Medical laser device recalled for inadequate safety operating instructions

    Ithera Medical is recalling the MSOT Acuity Echo medical laser device worldwide due to inadequate instructions for safe operation. Previous user manuals contained an incorrect Nominal Ocular Hazard Distance value.

    Product
    The MSOT Acuity Echo is a Class 4 medical laser device. The MSOT Acuity is a mobile assembly of electrically-powered components intended for imaging and analysis of soft-tissue and vasculature using combined optoacoustic (photoacoustic) and ultrasound (US) imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1141-2025·2025-02-19

    Spore Test Monitoring System Printing Error May Cause Result Misdirection

    HF Acquisition Co LLC is recalling Bio52 and Bio12 HealthFirst Mail In Monitoring Systems (4,021 units) due to a printing error on return envelopes that may cause spore test results to be reported to incorrect customer accounts.

    Product
    Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In Monitoring System, 12 Tests, Item: 1003580
    Category
    Medical Device
    Distribution
    50 states
  • HighFDA (Devices)·Z-1119-2025·2025-02-19

    Pyxis Medication and Anesthesia Dispensing Systems Recalled for Software Vulnerabilities

    CareFusion recalls Pyxis medication dispensing systems due to software issues that could delay access to medications, result in incorrect doses, or allow unauthorized access.

    Product
    (1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis CII Safe ES, Catalog No. 1116-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0538-2025·2025-02-19

    Chocolate Banana Granola Bars Recalled for Potential Metal Contamination

    Riverside Natural Foods is recalling Chocolate Banana Granola Bars sold nationwide due to potential metal contamination. Consumers should not eat affected products and should consult a healthcare provider if consumed.

    Product
    1. Chocolate Banana Granola Bars; 5.1oz (6 bars) 2. Chocolate Banana Granola Bars; 0.85oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0547-2025·2025-02-19

    Made Good Variety Pack recalled for potential metal contamination nationwide

    Riverside Natural Foods is recalling Made Good Variety Pack products nationwide due to potential metal contamination. Consumers should not consume the products and return them to retailers.

    Product
    1. Made Good Variety Pack 37ct 2.MadeGood Variety Pack 7ct
    Category
    Food
    Distribution
    Distributed nationwide