State

Tennessee product recalls

73,806 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.

Which agencies issued them

These figures cover only the 7,860 recalls whose distribution notice names Tennessee specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38026–38050 of 81666

HighFDA (Devices)·Z-1100-2019·2019-04-17
Edwards IntraClude Intra-Aortic Occlusion Device Recalled for Inter-Lumen Leak
Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices due to a reported leak between the cardioplegia and pressure lumens.
Product
Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a 10.5 Fr (3.5mm), triple lumen, 100cm long catheter with an elastomeric balloon near its distal tip designed to occlude the ascending aorta in order to partition the aortic root from arterial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1276-2019·2019-04-17
Trader Joe's Natural Creamer Recalled for Undeclared Milk Allergen
Good Karma Foods is recalling Trader Joe's Natural Creamer - Vanilla because the product contains milk but the label does not list it as an ingredient.
Product
PL Trader Joe Natural Creamer - Vanilla 12/32oz, Plastic bottle, Distributed by Good Karma Foods, Inc. with manufacturing at Shamrock Foods at Phoenix, AZ., Keep refrigerated
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1128-2019·2019-04-17
DePuy Orthopaedics Recalls CORAIL AMT COXA VARA Neck Segments
DePuy Orthopaedics is recalling CORAIL AMT COXA VARA Neck Segments because debris or material may be found behind the O-rings.
Product
CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1104-2019·2019-04-17
Abbott ARCHITECT c16000 Processing Module Recalled for Potential Incorrect Results
Abbott Laboratories is recalling 1,666 ARCHITECT c16000 Processing Modules worldwide because unresolved error codes may cause the instrument to generate incorrect diagnostic results.
Product
Abbott ARCHITECT c16000 Processing Module, List No. 03L77 - Product Usage: The Abbott ARCHITECT System is intended for In Vitro diagnostic use only. The Abbott ARCHITECT Clinical Chemistry Systems are designed to perform automated chemistry tests, utilizing photometry and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1120-2019·2019-04-17
Glenmark Recalls Pravastatin Sodium Tablets Due to Foreign Tablet Presence
Glenmark Pharmaceuticals is recalling 2,076 bottles of Pravastatin Sodium 20 mg tablets because a foreign tablet was found in the product.
Product
PRAVASTATIN SODIUM — PRAVASTATIN SODIUM (PRAVASTATIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1129-2019·2019-04-17
DePuy CORAIL AMT High Offset Neck Segment Recall for Potential Debris
DePuy Orthopaedics is recalling CORAIL AMT High Offset Neck Segments because debris or material may be found behind the O-rings.
Product
CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO), Pro. Code L20433 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1112-2019·2019-04-17
Siemens syngo.CT Cardiac Function Software Recalled for TAVI Measurement Risk
Siemens is recalling syngo.CT Cardiac Function software due to a potential risk of wrong measurement in the annulus plane during TAVI planning.
Product
syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT. Cardiac Function are image analysis software packages for evaluating cardiac CT angiography (CTA) volume sets. The software packages are designed to support the…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19737·2019-04-17
MTD Recalls Craftsman M350 Lawn Mowers Due to Injury Hazard
MTD is recalling about 5,000 Craftsman M350 walk-behind lawn mowers sold at Lowe's because sharp objects can pierce the collecting bag and strike users or bystanders.
Product
Craftsman M350 walk-behind lawn mowers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1102-2019·2019-04-17
Abbott ARCHITECT c4000 Processing Module Recalled for Potential Incorrect Results
Abbott Laboratories is recalling 3,675 ARCHITECT c4000 Processing Modules because specific unresolved error codes may cause the instrument to generate incorrect diagnostic results.
Product
Abbott ARCHITECT c4000 Processing Module, List No. 02P24 - Product Usage: The Abbott ARCHITECT System is intended for In Vitro diagnostic use only. The Abbott ARCHITECT Clinical Chemistry Systems are designed to perform automated chemistry tests, utilizing photometry and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1103-2019·2019-04-17
Abbott ARCHITECT c8000 Processing Module Recall for Potential Incorrect Results
Abbott is recalling 3,794 ARCHITECT c8000 Processing Modules because unresolved error codes may cause the instrument to generate incorrect diagnostic results.
Product
Abbott ARCHITECT c8000 Processing Module, List No. 01G06 - Product Usage: The Abbott ARCHITECT System is intended for In Vitro diagnostic use only. The Abbott ARCHITECT Clinical Chemistry Systems are designed to perform automated chemistry tests, utilizing photometry and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1115-2019·2019-04-17
Vygon DUALSTOP White Caps Recalled for Defect Causing Leaks
Vygon U.S.A. is recalling Vyon DUALSTOP White Caps used for intravascular lines because a defect causes leaks in the affected product.
Product
Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular lines.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V307000·2019-04-17
Livin' Lite Recalls Trailers With Blocked Emergency Exit Windows
Livin' Lite is recalling 2013-2017 Camplite and 2014-2017 Bearcat trailers because a manual awning arm may block an exit window, increasing injury risk during emergencies.
Product
LIVIN' LITE — LIVIN' LITE, LIVIN LITE CAMPLITE, BEARCAT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1112-2019·2019-04-17
FDA Recalls Life-Line Catalytic Activated Energy Water as Unapproved New Drug
McDaniel Life-Line LLC is voluntarily recalling Life-Line Catalytic Activated Energy Water because it is an unapproved new drug. The product was distributed in the US and several international countries.
Product
Life-Line tm Catalytic Activated Energy Water, 1 gallon container, McDaniel Life-Line LLC 1775 US Hwy 385 806-647-1741 Dimmitt, TX 79027
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1110-2019·2019-04-17
Procept Biorobotics Recalls AquaBeam Handpieces Due to Potential Internal Leaks
Procept Biorobotics is recalling 214 AquaBeam Handpieces because a micro-crack in a weld joint may cause an internal leak, potentially delaying or preventing the completion of medical procedures.
Product
AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301 distributed outside the U.S. Device Description The AQUABEAM Robotic System is intended for use in patients suffering from lower urinary tract symptoms resulting…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1127-2019·2019-04-17
DePuy CORAIL Neck Trials Recalled for Potential Debris Behind O-rings
DePuy Orthopaedics is recalling CORAIL AMT Standard Offset Neck Segments because debris or material may be found behind the O-rings. These surgical instruments are used in hip arthroplasty.
Product
CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1113-2019·2019-04-17
Siemens Medical Solutions Recalls syngo.via Cardiac Planning Software
Siemens Medical Solutions is recalling syngo.via syngo.CT Cardiac Planning software due to a potential risk of incorrect measurements during TAVI planning procedures.
Product
syngo.via syngo.CT Cardiac Planning, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT. Cardiac Function are image analysis software packages for evaluating cardiac CT angiography (CTA) volume sets. The software packages are designed to support the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2019·2019-04-17
Vygon DUALSTOP Red Caps Recalled for Defects Causing Leaks
Vygon U.S.A. is recalling 339,800 DUALSTOP Red Caps used for intravascular lines because a defect causes leaks.
Product
Vygon DUALSTOP Red Cap used for intravascular lines Product Code: 9888.00 - Product Usage: Cap used for intravascular lines.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V305000·2019-04-17
Spencer Fire Trucks Recalled for Brake Light Wiring Defect
Spencer Manufacturing is recalling certain 2017-2019 fire trucks because Whelen accessory brake lights may illuminate without the brake pedal being pressed.
Product
SPENCER — SPENCER FIRE TRUCK
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1120-2019·2019-04-17
Becton Dickinson Recalls Gravity IV Sets Due to Kinked Tubing
Becton Dickinson is recalling specific lots of Gravity IV Sets with 3-port Closed Stopcock Manifolds due to a confirmed complaint trend for kinked tubing.
Product
Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07
Category
Medical Device
Distribution
10 states
HighFDA (Devices)·Z-1109-2019·2019-04-17
Elekta Unity MRI Radiation Therapy System Recalled for Image Protocol Issues
Elekta Limited is recalling 12 Unity MRI-guided radiation therapy systems because acquired images may not represent average anatomy during respiratory motion, potentially affecting treatment accuracy.
Product
Elekta Unity, Image-Guided Radiation Therapy System Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19106·2019-04-17
Go Couture Recalls Children's Loungewear Due to Flammability Standard Violation
Go Couture is recalling about 120 children's loungewear sets because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.
Product
Children's loungewear sets
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1121-2019·2019-04-17
Becton Dickinson Recalls Gravity IV Sets Due to Kinked Tubing
Becton Dickinson is recalling specific lots of Gravity IV Sets with 3-port Closed Stopcock Manifolds due to a confirmed complaint trend for kinked tubing.
Product
Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07
Category
Medical Device
Distribution
10 states
ModerateFDA (Devices)·Z-1090-2019·2019-04-17
Integra bioBLOCK Resorbable Subtalar Implant Recalled for Temperature Exposure
Integra Limited is recalling 232 units of bioBLOCK Resorbable Subtalar Implants because temperature indicators suggest exposure to temperatures greater than 110°F.
Product
Integra bioBLOCK Resorbable subtaler Implant, 11mm Catalog Number: 040011 - Product Usage: The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1124-2019·2019-04-17
Roche COBAS INTEGRA 400 plus Recall for Carry-over Issues
Roche Diagnostics is recalling 656 COBAS INTEGRA 400 plus analyzers because specific tests require additional wash cycles to prevent carry-over.
Product
COBAS INTEGRA 400 plus analyzer used in the following assays: a)Tina-quant Apolipoprotein A-1 ver.2 Catalog Number: 03032566122 b)Tina-quant Albumin Gen.2 Catalog Number 04469658190 c)Creatinine plus ver.2 Catalog Number 03263991190 d) riglycerides Catalog Number…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1125-2019·2019-04-17
Roche cobas c 111 and COBAS INTEGRA 400 plus analyzers recalled for carry-over
Roche Diagnostics is recalling 137 cobas c 111 and COBAS INTEGRA 400 plus analyzers because specific tests require additional wash cycles to prevent carry-over.
Product
cobas c 111 with ISE analyzers analyzer used in the following assays: a)Creatinine plus ver.2 Catalog Number: 05401470190; b)Triglycerides Catalog Number: 04657594190 - Product Usage: Tina-quant Apolipoprotein A-1 ver.2 A lipoprotein test system is a device intended to…
Category
Medical Device
Distribution
Distributed nationwide