The Recall Desk

State

Tennessee product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45801–45825 of 81677

  • SevereFDA (Food)·F-3405-2017·2017-08-30

    Bush's Best Baked Beans Recalled for Defective Cans and Botulism Risk

    Bush Brothers & Co is recalling Bush's Best Baked Beans due to defective side seams that may allow C. botulinum growth.

    Product
    BUSHS BEST¿ Original SEASONED WITH BACON & BROWN SUGAR BAKED BEANS 28 OZ (1 LB 12 OZ) 794 g BUSH BROTHERS & COMPANY P. O. Box 52330, Dept, C KNOXVILLE, TN 37950-2330 UPC 0 39400 01614 4
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Drugs)·D-1121-2017·2017-08-30

    Major Senna Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3451-2017·2017-08-30

    Koogee-Queen Anne Recalls Ice Cream Due to E. coli Contamination

    Koogee-Queen Anne, LLC is recalling The Comfy Cow Strawberry Fields Forever Ice Cream due to E. coli and high Coliform Bacteria counts.

    Product
    The Comfy Cow Strawberry Fields Forever Ice Cream 1 pint
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-3403-2017·2017-08-30

    Bush's Best Baked Beans Recalled for Defective Cans and Botulism Risk

    Bush Brothers & Co is recalling Bush's Best Brown Sugar Hickory Baked Beans due to defective side seams that may allow C. botulinum growth.

    Product
    BUSH'S BEST¿ Brown Sugar Hickory SWEET HICKORY SAUCE WITH BROWN SUGAR & SPICES BAKED BEANS 28 OZ (1 LB 12 OZ) 794 g BUSH BROTHERS & COMPANY P. O. Box 52330, Dept, C KNOXVILLE, TN 37950-2330 UPC 0 39400 01977 0
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Drugs)·D-1120-2017·2017-08-30

    Rugby Diocto Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150. NDC: 0536-1001-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1122-2017·2017-08-30

    Rugby Aller-chlor Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1123-2017·2017-08-30

    Rugby Senexon Liquid Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, ?Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3054-2017·2017-08-30

    Medtronic AxiEM ENT Suction Devices Recalled for Verification Failure

    Medtronic is recalling 60 reusable ENT suction instruments because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.

    Product
    Medtronic Suction 9734308 Small AxiEM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3059-2017·2017-08-30

    Custom Assemblies Recalls Custom Surgical Kits with Defective BD Needles

    Custom Assemblies Inc is recalling 2,155 custom surgical kits because they contain BD SafetyGlide needles with loose polypropylene particulate in the fluid path.

    Product
    Various custom surgical kits manufactured for CMS, CUSTOM MEDICAL SPECIALTIES, INC.: (a) CMS-4153-R2 MPM Biopsy TRAY (b) CMS-5832-R1 Custom Safety Mammo Biopsy Tray (c) CMS-4108 Multipurpose Safety Tray (d) CMS-3141-R6 Custom Ultrasound Tray (e) CMS-2891-R1 Custom Safety…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3439-2017·2017-08-30

    Sysco X-Large Jo-Jo Wedges Recalled for Undeclared Milk

    Penobscot McCrum LLC is recalling Sysco X-Large Jo-Jo Wedges because the product may contain undeclared milk.

    Product
    Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighNHTSA·17V538000·2017-08-30

    REV Recalls 2018 Fleetwood and Holiday Rambler Motorhomes for Wiring Defect

    REV is recalling 2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because improperly stripped generator wires may cause an electrical short and fire.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER JAMBOREE, VESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3066-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans SFILL 360 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans SFILL 360 devices because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans SFILL 360, 3-TT-SFILL 360. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3049-2017·2017-08-30

    Alcon ORA System Recall for Incorrect IOL Power Measurements

    Alcon is recalling 429 ORA Systems with VerifEye+ Carts due to a software error that may cause incorrect intraocular lens power measurements during cataract surgery.

    Product
    ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3061-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 250 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 250 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3052-2017·2017-08-30

    Medtronic Curved Suction 70 Recalled for Verification Failure

    Medtronic is recalling 149 Curved Suction 70 ENT instruments because they fail required pre-use verification checks.

    Product
    Medtronic Curved Suction 70 9733450 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3063-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 1000 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 1000 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 1000, 3-TT-FILTRON 1000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3437-2017·2017-08-30

    Penobscot McCrum Recalls Seasoned Jo-Jo Wedges for Undeclared Milk

    Penobscot McCrum LLC is recalling Extra Large Seasoned/Battered Jo-Jo Wedges because the product may contain undeclared milk.

    Product
    Extra Large Seasoned/Battered Jo-Jo Wedges / 00148 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-3064-2017·2017-08-30

    FDA Recalls Tissu-Trans Filtron 2000 Due to Sterile Seal Integrity Concerns

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 2000 because the sterile package seal integrity cannot be assured.

    Product
    Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3438-2017·2017-08-30

    Valero Baby Wedges Recalled for Undeclared Milk

    Penobscot McCrum LLC is recalling Valero Baby Wedges with Crisp Coat UC Coating because the product may contain undeclared milk.

    Product
    Valero Baby Wedges with Crisp Coat UC Coating / 51049 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-3065-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans MEGA 1500 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 devices because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans MEGA 1500, 3-TT-MEGA 1500. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3058-2017·2017-08-30

    Medtronic ENT Navigation Suction Devices Recalled for Verification Failure

    Medtronic Navigation is recalling six kits of ENT suction devices because they fail required pre-use verification checks.

    Product
    Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM, reusable, Rx. This kit includes 9733908 (which includes 9733452 containing 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 deg Curved Suction). The firm name on the label is Medtronic Navigation, Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide