State
72,986 recalls have nationwide distribution and so reach Tennessee. 7,821 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,821 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,653 (21%) are Severe.
Which agencies issued them
These figures cover only the 7,821 recalls whose distribution notice names Tennessee specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dlesot Snap Hair Clips contain lead paint levels exceeding the federal ban, posing a lead poisoning hazard to children. Approximately 3,800 units were sold on Amazon from April through September 2024.
Santa Cruz Bicycles is recalling about 2,850 Heckler 9 electric bicycles due to a fire hazard in the lithium-ion battery. The firm has received three reports of fires with some property damage but no reported injuries.
Kohl's is recalling about 1,960 St. Nicholas Square Christmas Tea Light Candle Holders because they can catch on fire, posing a fire and burn hazard. Two fires have been reported with no injuries.
Kubota is recalling about 49,640 RTV-series utility vehicles because the ball joint on the front suspension can loosen and separate, causing drivers to lose wheel support and risking a crash. No injuries have been reported.
Brinkley RV is recalling 2024-2025 Model G and Model Z fifth-wheel trailers with potentially detaching step assemblies. The clip-on bracket bolts may loosen, causing steps to detach and increasing injury risk.
Keystone is recalling certain 2025 Kodiak travel trailers because the patio support struts may not adequately support the fold-down patio's weight, increasing the risk of injury. Owners should contact Keystone or their dealer for free repair.
Jayco is recalling 2025 Entegra Launch and Terrain motorhomes because a standard outlet was installed in the kitchen instead of a GFCI protected outlet, increasing the risk of electric shock.
USDA FSIS issued a public health alert for mixed potato chip products containing pork cracklings imported from Colombia, a country ineligible to export meat to the U.S.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The affected product was distributed nationwide.
Abbott is recalling specific lots of the Amplatzer TorqVue LP Delivery System due to a possible small breach in the shaft that is not visible but could lead to prolonged procedures, blood loss, or air embolism.
Denver Solutions, LLC DBA Leiters Health is recalling PHENYLephrine HCl 0.5 mg per 5mL single-dose syringes because some syringes may be leaking or damaged, which could compromise sterility assurance.
Leiters Health is recalling dexmedetomidine HCl PF syringes nationwide due to leaking or damaged syringes that may not maintain sterility. Affected lot 2431276A has an expiration date of 4/20/2025.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection vials nationwide because some media fill units showed bacterial contamination, indicating a lack of sterility assurance. The affected product is a 100mg/mL injectable antipsychotic medication.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The drug is used for intramuscular injection to treat psychiatric conditions.
Denver Solutions, LLC is recalling Ketamine HCl 50mg per 5mL single-dose syringes nationwide due to leaking or damaged syringes that may lack sterility assurance. Two affected lots are identified with expiration dates in July 2025.
Abbott is recalling the Amplatzer TorqVue LP Catheter (Model 9-TVLPC4F90/080) due to a potential small breach in the proximal shaft that may not be visible and could lead to prolonged procedures, blood loss, or air embolism.
Denver Solutions, LLC DBA Leiters Health is recalling Rocuronium Bromide 50 mg per 5mL syringes due to potential leaking or damage that may compromise sterility assurance.
Medtronic MiniMed is recalling InPen smart insulin pens that may have been incorrectly assembled, potentially causing the insulin cartridge to not fit or the cartridge holder to be difficult to remove. Users without backup insulin could experience temporary hyperglycemia.
CareFusion's BD PYXIS MEDBANK and MEDFLEX automated dispensing cabinets may experience a software issue during bin restocking that doubles bin quantities, potentially delaying access to medications and supplies.
Philips is recalling Brilliance CT Big Bore computed tomography systems due to unintended motion in the interventional control that may cause the gantry or table to collide with operators or patients.
Maquet Cardiovascular is recalling the VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System due to a ceramic C-Ring component that may break during use. At least 12 user complaints were reported as of March 3, 2025.
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because a software defect allows expired reagents to be used without user notification. The system may incorrectly update expiration dates to current or future dates, contrary to the operator's manual.
Denver Solutions, LLC (DBA Leiters Health) is recalling Glycopyrrolate 1mg/5mL single-dose syringes (Lot #2431015B, expiration 4/10/2025) distributed nationwide because some syringes were found to be leaking or damaged, which compromises sterility assurance.
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because expired reagents may be used without user notification when scanned or manually entered into the system, contrary to manufacturer guidelines.
Abbott's CELL-DYN Ruby hematology analyzer may accept expired reagents without alerting the operator, potentially allowing use of expired materials in patient testing.