The Recall Desk

State

Tennessee product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29851–29875 of 81596

  • SevereFDA (Devices)·Z-0230-2021·2020-10-28

    ICU Medical Recalls 114-inch Burette Sets Due to Seal Defect

    ICU Medical is recalling specific lots of 114-inch burette sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.

    Product
    114" (290 cm) 60 Drop 150ml Burette Set (Clave, Shut Off, Filter) w/4 Clave Remv 3-Port NanoClave Manifold, 2 Check Valves, Rotating Luer, 2 Exts. 1 unit per pouch, 25 pouches per case.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0177-2021·2020-10-28

    Bien-Air Surgery Multifunction Pedal Recalled Due to Magnet Failure Risk

    Bien-Air Surgery is recalling 1,120 OsseoDuo multifunction foot pedals because an internal magnet may detach, causing the motor to start unattended and become unstoppable.

    Product
    Bien-Air Surgery REF 1600517-001 SN ******* MULTIFUNCTION PEDAL OSSEODUO - Product Usage: Product Usage: intended to convert electrical energy to mechanically drive attachment, microsaws, shaver blades and burs, burs and perforator tools for cutting and shaping bone including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0052-2021·2020-10-28

    Sauer Brands Recalls Szechwan Seasoning Due to Salmonella Risk

    Sauer Brands Inc is recalling The Spice Hunter Szechwan Seasoning due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    The Spice Hunter Szechwan Seasoning 2.1 oz. Jar UPC 8105701955 Case UPC 40081057019557
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0179-2021·2020-10-28

    Stryker S2 Mini Foot Pedal Recalled Due to Magnet Defect

    Bien-Air Surgery is recalling Stryker S2 Mini Foot Pedals because an internal magnet may detach, causing the motor to start unattended and become unstoppable.

    Product
    Stryker Instruments REF 5452-007-000 SN ******* S2 MINI FOOT Pedal - Product Usage: The S2 Mini Drill System has been designed for the light drilling of bones as part of surgical operations such as stapedotomy or ossiculoplasty. The S2 Mini Drill System consists of a foot…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0089-2021·2020-10-28

    Medtronic Vascular Recalls Rashkind Balloon Septostomy Catheters Due to Field Failures

    Medtronic Vascular is recalling 505 units of Rashkind Balloon Septostomy Catheters due to subsequent field failures and failed quality testing.

    Product
    Rashkind Balloon Septostomy Catheter, 4F, Closed end, 50 cm, Pediatric, Single Lumen Product number: 007161 GTIN: 00613994760272 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial septal defect as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0087-2021·2020-10-28

    Medtronic Rashkind Balloon Septostomy Catheter Recall for Quality Failures

    Medtronic Vascular is recalling Rashkind Balloon Septostomy Catheters due to field failures and failed quality testing. The recall covers 2,356 units distributed worldwide.

    Product
    Rashkind Balloon Septostomy Catheter, 6F, Recess Balloon, Closed end, 50 cm, Pediatric, Single Lumen Product number: 008764 GTIN: 00613994760289 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0129-2021·2020-10-28

    GE Healthcare Recalls MRI Systems Due to Electrical Arc Flash Risk

    GE Healthcare is recalling 30 MRI systems worldwide due to a potential electrical arc flash hazard within the power cabinet.

    Product
    System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0056-2021·2020-10-28

    Sauer Brands Recalls Malabar Black Peppercorns Due to Salmonella Risk

    Sauer Brands is recalling Malabar Black Peppercorns due to potential Salmonella contamination. Consumers should stop using the product and return it to the store of purchase.

    Product
    The Spice Hunter Malabar Black Peppercorns 2.1 oz. Jar UPC 8105701700 Case UPC 40081057017003
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0128-2021·2020-10-28

    GE Healthcare Recalls MRI Systems Due to Electrical Arc Flash Risk

    GE Healthcare is recalling 30 MRI systems worldwide due to a potential electrical arc flash hazard within the power cabinet.

    Product
    System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V663000·2020-10-28

    Daimler Recalls 2015-2020 Sprinter Vans for Steering Hose Defect

    Daimler Vans USA is recalling 2015-2020 Mercedes-Benz and Freightliner Sprinter vans because hydraulic power steering hoses may detach, causing fluid leaks and loss of steering assist.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0118-2021·2020-10-28

    Smith & Nephew Recalls Genesis Knee Implants Due to Design Defect

    Smith & Nephew is recalling 47 Genesis knee implants because the anterior locking detail does not meet design specifications.

    Product
    Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are absent or incompetent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0064-2021·2020-10-28

    Sauer Brands Recalls Holiday Spice Shipper Boxes Due to Salmonella Risk

    Sauer Brands Inc is recalling specific holiday spice shipper boxes nationwide and online due to potential Salmonella contamination.

    Product
    Shipper boxes - sent to retail stores for display. Spices contained in the boxes are currently under recall. Thanksgiving shipper - item # 43149 Holiday Gourmet Shipper - Item # 43142 Shipper - Organic Holiday - Item # 43143
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0119-2021·2020-10-28

    Olympus Choledoscope Recalled for Lack of Clearance and Breakage

    Olympus is recalling CHF-CB30S choledoscopes because they lack FDA clearance and have experienced breakage and metal protrusion during use.

    Product
    Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light source, TV monitor, endo-therapy accessories and other ancillary equipment for endoscopic diagnosis and treatment within the biliary tract (common bile…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0189-2021·2020-10-28

    ICU Medical Recalls Smallbore Bifuse Extension Sets Due to Seal Defect

    ICU Medical is recalling specific lots of 9-inch Smallbore Bifuse Extension Sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.

    Product
    9" (23 cm) Appx 0.63 ml, Smallbore Bifuse Ext Set w/2 MicroClave Clear, NanoClave, 3 Clamps, 0.2 Micron Filter, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case UDI:(01)10887709052953(17)241201(30)50(10)4536611;(01)10887709052953(17)250101(30)50(10)4557492 The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0050-2021·2020-10-28

    Sauer Brands Recalls Mexican Seasoning for Potential Salmonella Contamination

    Sauer Brands Inc is recalling The Spice Hunter Mexican Seasoning due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Mexican Seasoning 1.4 oz. Jar UPC 8105701541 Case UPC 40081057015412
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0057-2021·2020-10-28

    Sauer Brands Recalls Freeze-Dried Chives Due to Salmonella Risk

    Sauer Brands Inc is recalling The Spice Hunter Freeze-Dried Chives due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    The Spice Hunter Freeze-Dried Chives 0.13 oz. Jar UPC 8105701230 Case UPC 40081057012305
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0127-2021·2020-10-28

    GE Healthcare Recalls MRI Systems Due to Potential Electrical Arc Flash

    GE Healthcare is recalling 30 MRI systems due to a potential electrical arc flash hazard within the Power Gradient & RF cabinet.

    Product
    System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0088-2021·2020-10-28

    Medtronic Recalls Rashkind Balloon Septostomy Catheters Due to Field Failures

    Medtronic Vascular is recalling 711 units of Rashkind Balloon Septostomy Catheters due to subsequent field failures and failed quality testing.

    Product
    Rashkind Balloon Septostomy Catheter, 5F, Closed end, 50 cm, Pediatric, Single Lumen Product number: 007160 GTIN: 00613994760265 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial septal defect as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0046-2021·2020-10-28

    Sauer Brands Recalls Coriander Jars Due to Potential Salmonella Contamination

    Sauer Brands Inc is recalling The Spice Hunter Coriander jars due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Coriander 1.4 oz. Jar UPC 8105701275 Case UPC 40081057012756
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0255-2021·2020-10-28

    ICU Medical Recalls Intravascular Administration Sets Due to Manufacturing Defect

    ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect on the NanoClave may prevent a proper seal with the spike.

    Product
    148 IN (376cm) APPX 18.8 ml, 15 DROP SET, 2 CLAVE, Remv 3 Gang Clave Stopcock.1 unit per pouch, 25 pouches per case. UDI:(01)10887709071558(17)250101(30)25(10)4603841. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0222-2021·2020-10-28

    ICU Medical Recalls Intravascular Administration Sets Due to Seal Defect

    ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent a proper seal.

    Product
    123 IN (312cm) APPX 16.1 ml, 10 DROP SET w/3 MicroClave, 3-Port NanoClave; UDI:(01)10887709085432(17)241201(30)25(10)4536733;(01)10887709085432(17)250101(30)25(10)4573641. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0130-2021·2020-10-28

    GE Healthcare Recalls MRI Systems Due to Electrical Arc Flash Risk

    GE Healthcare is recalling 30 MRI systems worldwide due to a potential electrical arc flash hazard within the Power Gradient & RF Cabinet.

    Product
    System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0059-2021·2020-10-28

    Sauer Brands Recalls The Spice Hunter Cilantro Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling The Spice Hunter Cilantro jars due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Cilantro 0.3 oz. Jar UPC 8105701236 Case UPC 40081057012367
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0040-2021·2020-10-28

    Sauer Brands Recalls Saigon Organic Cinnamon Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling Saigon Organic Cinnamon jars due to potential Salmonella contamination. The product was sold nationwide and online.

    Product
    The Spice Hunter Saigon Organic Cinnamon 1.7 oz. Jar UPC 8105701245 Case UPC 40081057012459
    Category
    Food
    Distribution
    Distributed nationwide