State

Tennessee product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35976–36000 of 81600

HighFDA (Devices)·Z-2271-2019·2019-08-21
Siemens SOMATOM Drive CT Systems Recalled for Software Safety Issues
Siemens Medical Solutions is recalling SOMATOM Drive CT systems due to four software issues that may cause scan aborts.
Product
SOMATOM Drive, Model Number 10431700 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V612000·2019-08-21
Rolls-Royce Cullinan Recall for Dim Brake Lights
BMW is recalling 2019 Rolls-Royce Cullinan vehicles because brake lights may not be bright enough, increasing crash risk.
Product
ROLLS-ROYCE — ROLLS-ROYCE CULLINAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2270-2019·2019-08-21
Siemens SOMATOM CT Systems Recalled for Software Scan Abort Risk
Siemens is recalling SOMATOM Definition Flash CT systems due to four software issues that may cause scans to abort.
Product
SOMATOM Definition Flash, Model Number 10430603 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2248-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x36 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x36, Item Number 19654 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2268-2019·2019-08-21
Siemens SOMATOM Definition AS CT Systems Recalled for Software Issues
Siemens Medical Solutions USA is recalling SOMATOM Definition AS CT systems due to four safety-related software issues in syngo.CT version VB10A that may cause scan aborts.
Product
SOMATOM Definition AS, Model Number 8098027 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2256-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x110 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x110, Item Number 19670 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2244-2019·2019-08-21
BioPro K-Wire Single Trocar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 350 units of K-Wire Single Trocar 1.1x150mm due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Single Trocar 1.1x150mm, Item Number OL15011S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2250-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x34 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x34, Item Number 19653 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2243-2019·2019-08-21
BioPro K-Wire Single Trocar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling 350 units of K-Wire Single Trocar 1.6x150mm due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Single Trocar 1.6x150mm, Item Number OL15016S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2241-2019·2019-08-21
BioPro K-Wire Sterile Single Trochar Recalled for Sterile Barrier Flaw
BioPro, Inc. is recalling K-Wire Sterile Single Trochar units due to a manufacturing flaw in the sterile barrier system.
Product
K-Wire Sterile Single Trochar .045, Item Number 19108 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2252-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x90 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x90, Item Number 19666 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2273-2019·2019-08-21
Siemens SOMATOM Edge Plus CT Systems Recalled for Software Issues
Siemens is recalling SOMATOM Edge Plus CT systems due to four safety-related software issues in syngo.CT version VB10A that may cause scan aborts.
Product
SOMATOM Edge Plus, Model Number 10267000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2257-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x120 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x120, Item Number 19672 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2247-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x100 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x100, Item Number 19668 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2251-2019·2019-08-21
BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x85 due to a manufacturing flaw in the sterile barrier system. The devices were distributed in the US and internationally.
Product
Go-EZ Screw 6.5x85, Item Number 19665 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2287-2019·2019-08-21
Luminex Recalls ARIES C. difficile Assay Due to Seal Defects
Luminex is recalling ARIES C. difficile Assay kits because defective side cassette seals may reduce assay sensitivity and stability.
Product
ARIES C. difficile Assay , REF 50-10018, UDI # 00840487100059
Category
Medical Device
Distribution
34 states
HighFDA (Devices)·Z-2272-2019·2019-08-21
Siemens SOMATOM Confidence CT Systems Recalled for Software Safety Issues
Siemens Medical Solutions is recalling SOMATOM Confidence CT systems due to four software issues that may cause scan aborts.
Product
SOMATOM Confidence, Model Number 10590100 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2269-2019·2019-08-21
Siemens CT Systems Recalled for Software Issues Causing Scan Aborts
Siemens is recalling SOMATOM Definition Edge CT systems due to four safety-related software issues in syngo.CT version VB10A that may result in scan aborts.
Product
SOMATOM Definition Edge, Model Number 10590000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2279-2019·2019-08-21
BD Vacutainer Fluoride Tubes Recalled Due to Missing Preservative Additive
Becton Dickinson is recalling 247,000 blood alcohol test tubes because they lack the required fluoride additive, which may cause inaccurate test results if samples are stored for more than two days.
Product
BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol determinations
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2274-2019·2019-08-21
Siemens SOMATOM Force CT Systems Recalled for Software Scan Abort Issues
Siemens Medical Solutions is recalling SOMATOM Force CT systems due to four software issues that may cause scan aborts.
Product
SOMATOM Force, Model Number 10742326 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2255-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Manufacturing Flaw
BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x105 (Item 19669) due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x105, Item Number 19669 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2278-2019·2019-08-21
Pega Medical Recalls SLIM Handle Components Due to Jamming Risk
Pega Medical Inc. is recalling 19 SLIM Handle components because an internal ring may detach, causing the handle to jam with the driver.
Product
SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System
Category
Medical Device
Distribution
8 states
HighFDA (Food)·F-1990-2019·2019-08-21
Entenmann's Little Bites Cookies Recalled for Possible Plastic Pieces
BIMBO Bakeries USA Inc. is recalling 160,000 boxes of Entenmann's Little Bites Soft Baked Cookies due to a manufacturing failure that may have introduced small plastic pieces into the product.
Product
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5 pouches per package, package type is carton, units per case 12
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-2249-2019·2019-08-21
BioPro Go-EZ Screw Recalled Due to Sterile Barrier Flaw
BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x95 due to a manufacturing flaw in the sterile barrier system.
Product
Go-EZ Screw 6.5x95, Item Number 19667 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2284-2019·2019-08-21
Luminex ARIES Flu A/B & RSV Assay Recalled for Seal Defects
Luminex is recalling ARIES Flu A/B & RSV Assay kits because a seal defect may reduce assay sensitivity or stability.
Product
ARIES Flu A/B & RSV Assay , REF 50-10020, UDI # 00840487100158
Category
Medical Device
Distribution
34 states