State
73,718 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.
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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sun Pharmaceutical Industries Inc. is recalling 13,834 bottles of Riomet (metformin hydrochloride) oral solution due to microbial contamination of the non-sterile product.
Novo Nordisk is recalling specific samples of Insulin Diluting Medium for NovoLog because they were stored below 32°F, potentially causing lack of efficacy and damage to the cartridge and pen-injectors.
Siemens Healthcare is recalling 132 ADVIA 2120 hematology analyzers because a software defect may cause sample identification mismatches with 14-character barcodes.
Volkswagen is recalling 2021 Arteon vehicles because incorrectly calibrated tire pressure sensors may fail to detect low air pressure, increasing crash risk.
BRAV USA is recalling Swix Focus Down Jackets Jr. because hood and waist drawstrings pose strangulation and entrapment risks to children.
Siemens is recalling 187 ADVIA 2120i Dual Aspirate Autosamplers due to a potential sample identification mismatch with 14-character barcodes.
Akron Brass is recalling Weldon V-Mux Vista IV LCD displays used in emergency vehicles due to a defect that may cause the screen to lock up or become nonfunctional.
Metal Ware is recalling NESCO Coffee Bean Roasters because they can overheat and cause fires. Consumers should stop using the units and contact the company for a refund.
Siemens is recalling 7 ADVIA 2120 automated hematology analyzers due to a potential sample identification mismatch with 14-character barcodes.
Siemens is recalling 15 ADVIA 2120i automated hematology analyzers because a software defect may cause sample identification mismatches with 14-character barcodes.
Siemens Healthcare is recalling 674 ADVIA 2120i Dual Aspirate Autosamplers due to a potential sample identification mismatch with 14-character barcodes.
Siemens is recalling ADVIA 2120 Autosamplers due to a potential sample identification mismatch with 14-character barcodes.
Stryker is recalling PINPOINT Video Processors/Illuminators that may flicker, lose image, or reboot unexpectedly.
2022 Kia Carnival vehicles may have damaged fuel rail tubes that could leak fuel, increasing the risk of fire. Kia will inspect and replace affected fuel rails free of charge.
Medline Industries is recalling Stat-Site B-HB Diluent because shipment compromise may cause false test results.
Brompton Bicycle Inc. is recalling about 600 electric folding bicycles because a software malfunction can cause the motor to continue providing assistance when the rider is not pedaling, posing fall and injury hazards.
Siemens is recalling 32 ADVIA 2120 Dual Aspirate Autosamplers due to a potential sample identification mismatch with 14-character barcodes.
Siemens Healthcare Diagnostics is recalling 572 ADVIA 2120i automated hematology analyzers due to a potential sample identification mismatch with 14-character barcodes.
Siemens Healthcare Diagnostics is recalling 8 ADVIA 2120i automated hematology analyzers due to a potential sample identification mismatch with 14-character barcodes.
Airstream is recalling 2020-2021 Interstate vehicles because the Gross Vehicle Weight Rating label may list incorrect occupant cargo capacity, potentially leading to vehicle overload.
Siemens is recalling 43 ADVIA 2120 automated hematology analyzers worldwide due to a potential sample identification mismatch with 14-character barcodes.
Siemens Healthcare Diagnostics is recalling 185 ADVIA 2120i Dual Aspirate Autosamplers due to potential sample identification mismatches with 14-character barcodes.
Roche is recalling cobas SARS-CoV-2 & Influenza A/B assay reagents because they may produce invalid or false positive results.
Siemens Healthcare Diagnostics is recalling ADVIA 2120i automated hematology analyzers because 14-character barcodes may cause sample identification mismatches.
Siemens Healthcare Diagnostics is recalling 195 ADVIA 2120 automated hematology analyzers worldwide due to a potential sample identification mismatch with 14-character barcodes.