State

Tennessee product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31326–31350 of 81597

SevereFDA (Drugs)·D-1358-2020·2020-07-08
Koala Hand Sanitizer Recalled for Subpotent Ethanol and Undeclared Isopropyl Alcohol
Beaming White LLC is recalling Koala Hand Sanitizer because the active ingredient ethanol was tested below the label claim and undeclared isopropyl alcohol was present.
Product
Koala Hand Sanitizer, Menthol, 16 FL OZ., Antibacterial, (Ethyl Alcohol 69%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1019-2020·2020-07-08
Trident Seafoods Recalls Imitation Crab Supreme Due to Undeclared Egg
Trident Seafoods is recalling Gordon Choice Imitation Crab Supreme Style because the product may contain undeclared egg white.
Product
Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution exclusively by Gordon Food Service Wyoming, MI 49509
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·20V399000·2020-07-08
Kia Recalls 2020 Sedona Vehicles Due to Alternator Fire Risk
Kia is recalling 2020 Sedona vehicles because a loose alternator terminal nut may cause electrical arcing and increase the risk of a fire.
Product
KIA — KIA SEDONA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2451-2020·2020-07-08
LivaNova Recalls Sterile Connectors Due to Potential Barrier Breach
LivaNova USA Inc. is recalling 600 units of sterile disposable connectors because internal tests found the sterile barrier may be breached.
Product
Sterile Disposable Connectors ASY CONN REDUCER 3/8 X 1/4 24 REF/ GTIN for Insert Label:050516000/ 00803622123276
Category
Medical Device
Distribution
44 states
SevereFDA (Devices)·Z-2455-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY Y CONN 3/8 X 3/8 X 3/8 24 REF/ GTIN for Insert Label:050526000/ 00803622123320
Category
Medical Device
Distribution
44 states
HighFDA (Food)·F-1014-2020·2020-07-08
Brill Frozen Cookie Dough Recalled for Undeclared Walnuts
Brill Inc. is recalling 252 cases of frozen cookie dough because the product may contain undeclared walnuts, a major food allergen.
Product
Brill 30 lb. cases of 480 1.0 oz. chocolate chip with mini colored candy pieces frozen cookie dough, MDM # 10194626, Manufactured by Brill, Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2459-2020·2020-07-08
LivaNova Recalls 220 Units of 3/8 Inch Y Connectors
LivaNova USA Inc. is voluntarily recalling 220 units of 3/8 inch Y connectors due to a Class II defect.
Product
3/8X3/8X3/8 Y CONN, STRL REF/ GTIN for Insert Label:EC2105S/ 00803622129285
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2462-2020·2020-07-08
LivaNova Recalls Sterile Standalone Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling 240 units of sterile standalone connectors because internal tests found potential breaches in the sterile barrier.
Product
1/2 - 3/8 REDUC CONN, STRL REF/ GTIN for Insert Label:EC2145S/ 00803622129322
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2453-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY CONN EQUAL 3/16 WYE 24 REF/ GTIN for Insert Label:050523000/ 00803622123290
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2437-2020·2020-07-08
Siemens CentraLink Software Recalled for Potential Erroneous Patient Results
Siemens Healthcare Diagnostics is recalling CentraLink Data Management System software versions 16.0.2 and 16.0.3 due to a defect that may cause erroneous patient results.
Product
(1) CentraLink Data Management System software version 16.0.2 Siemens Material Number (SMN): 11313246 (2) CentraLink Data Management System software version 16.0.3 Siemens Material Number (SMN): 11314337 Product Usage: are clinical laboratory information modules which…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2456-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling 768 units of Sterile Disposable Connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY RDC Y 1/2X3/8X3/8 STR 24 REF/ GTIN for Insert Label:050529000/ 00803622123351
Category
Medical Device
Distribution
44 states
HighCPSC·20146·2020-07-08
Lidl Recalls Silvercrest Bread Makers Due to Electric Shock Hazard
Lidl US is recalling approximately 1,840 Silvercrest bread makers because the lid can become energized, posing an electric shock hazard.
Product
Silvercrest Bread Makers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2443-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Potential Barrier Breach
LivaNova USA Inc. is recalling 120 units of sterile disposable connectors because internal tests found the sterile barrier may be breached.
Product
Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ GTIN for Insert Label:029165000/ 00803622123153
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2479-2020·2020-07-08
Preventice BodyGuardian Heart Remote Monitoring Kit Recalled for Data Accuracy Issues
Preventice Services is recalling eight BodyGuardian Heart Remote Monitoring Kits because unvalidated software may cause inaccurate data collection, making patient reports unreliable for condition evaluation.
Product
BodyGuardian Heart Remote Monitoring Kit, consisting of two BG Heart monitors, either Models BC-1001-A or BC1001-D, and a cell phone, either Models BP1008 or BP10014, that is paired to both of the monitors.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20E047000·2020-07-08
TAP Recalls Rubicon Express Suspension Lift Kits for Jeep Gladiator
TAP Worldwide is recalling certain Rubicon Express suspension lift kits for 2020-2021 Jeep Gladiators because the fitment guide inaccurately lists 40-inch tires as compatible, which can affect vehicle stability.
Product
TIRES recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2468-2020·2020-07-08
Radiometer ABL80-FLEX CO-OX Box Label Recall for Barcode Misinterpretation
Radiometer Medical ApS is recalling ABL80-FLEX CO-OX box labels because barcode misinterpretation on analyzers may cause patient mix-ups or delayed treatment.
Product
ABL80-FLEX CO-OX 393-841 Box Label, REF 393-841, IVD, CE, UDI: 05700693938417 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2450-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling 96 units of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY S/1/4 TO 3/16 RED 24 REF/ GTIN for Insert Label:050514000/00803622123269
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2458-2020·2020-07-08
LivaNova Recalls Sterile Standalone Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling 20 units of Sterile Standalone Connectors because internal tests identified potential breaches in the sterile barrier.
Product
1/4X3/16X3/16YCONN,STRL REF/ GTIN for Insert Label:EC2102S/ 00803622129278
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2447-2020·2020-07-08
LivaNova Recalls Sterile Standalone Connectors Due to Potential Barrier Breach
LivaNova USA Inc. is recalling specific lots of sterile standalone connectors because internal tests found the sterile barrier may be breached.
Product
Sterile Disposable Connectors ASY STR CONN 1/4 STRLE 24. REF/ GTIN for Insert Label:050504000/ 00803622123221
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2470-2020·2020-07-08
Siemens IMMULITE 2000 XPi Analyzer Recalled for Tubing Crack Risk
Siemens Healthcare Diagnostics Inc. is recalling 2,925 IMMULITE 2000 XPi Immunoassay Systems because flexible tubing can crack, causing liquid waste leaks and slip hazards.
Product
Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Analyzer SMN #10373214 - Product Usage: are intended for professional use in a laboratory environment only.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2469-2020·2020-07-08
Siemens IMMULITE 2000 Analyzer Recalled for Tubing Crack Hazard
Siemens Healthcare Diagnostics is recalling 1,555 IMMULITE 2000 analyzers because flexible tubing can crack, causing liquid waste leaks and slip hazards.
Product
Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer SMN #10380062 - Product Usage: are intended for professional use in a laboratory environment only.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1011-2020·2020-07-08
Simply Nature Sweet Potato Bites Recalled for Foreign Object Risk
Dr. Praeger's is recalling Simply Nature Sweet Potato Bites because the product may contain a foreign object. Consumers should check their pantries for the specific lot code.
Product
Simply Nature Sweet Potato Bites, 12oz retail boxes variety pack, Expiration date 4/9/2022. Lot code R20AJ-01A.
Category
Food
Distribution
30 states
HighFDA (Devices)·Z-2445-2020·2020-07-08
LivaNova Recalls Sterile Disposable Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Product
Sterile Disposable Connectors ASY 1/4 X 3/8 REDUCER W/LL 24. REF/ GTIN for Insert Label:050434000/ 00803622123207
Category
Medical Device
Distribution
44 states
HighCPSC·20145·2020-07-08
GloryBee Wintergreen Essential Oil Recalled for Packaging Defect
GloryBee Natural Sweeteners is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Product
GloryBee Wintergreen Essential Oil
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2460-2020·2020-07-08
LivaNova Recalls Sterile Standalone Connectors Due to Barrier Breach
LivaNova USA Inc. is recalling 860 units of Sterile Standalone Connectors because internal tests identified a potential breach in the sterile barrier.
Product
3/8 STR CONN, STRL REF/ GTIN for Insert Label:EC2130S/ 00803622129292
Category
Medical Device
Distribution
44 states