State
73,827 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.
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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Integra LifeSciences is recalling Cranial Access Kits because product seals may open during distribution, rendering the devices unsterile.
Maquet is recalling Connecting Bracket (Fixture) Devices because post-market surveillance reports indicate the welded joint between the square mount and the first fixable swivel joint is broken.
Pharmavite is recalling specific lots of Nature Made adult gummies Multi due to possible Salmonella contamination.
Pharmavite is recalling specific lots of Nature Made Multi + Omega-3 supplements due to possible Salmonella contamination. Consumers should stop using the affected products.
Geneva Foods is recalling Lysander's Premium Teriyaki Marinade because it contains undeclared soy, wheat, and sulfites.
Hospira is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms or therapy interruption.
Amerisource Health Services is recalling 867 cartons of 20 mg amphetamine tablets due to unit dose blister cavities containing more than one tablet.
Geneva Foods is recalling Lysander's All Natural Bourbon Flavor Rub because it contains undeclared soy, wheat, and sulfites.
Pharmavite is recalling specific lots of Nature Made adult gummies Multi due to possible Salmonella contamination. Consumers should check lot numbers and expiration dates.
Pharmavite is recalling Nature Made Super B-Complex vitamins due to possible Staphylococcus aureus and Salmonella contamination in specific lots.
Pharmavite is recalling Nature Made Super B-Complex supplements due to possible Staphylococcus aureus and Salmonella contamination in specific lots.
Hologic is recalling 1,440 SureSight Obturator Introducer Localization Systems because the tip may break at the glue joint.
Philips is recalling three BrightView XCT Upgrade units due to a software defect that may cause the detector to contact patients during specific scans.
Hospira Inc. is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.
Terumo Medical Corporation is recalling Pinnacle Introducer Sheaths due to a manufacturing issue causing valve leakage, which poses a risk of incremental blood loss.
Riverpoint Medical is recalling specific lots of Webglo polypropylene surgical sutures because the seals may open during distribution or packaging.
Blackrock Microsystems is recalling 81 Neural Signal Amplifiers because the device and patient cable are incorrectly labeled as Type CF Applied Parts.
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Blackrock Microsystems is voluntarily recalling 120 Patient Cables because they are incorrectly labeled as Type CF Applied Parts.
Zydus Pharmaceuticals is recalling 14,808 bottles of Bromocriptine Mesylate 5 mg capsules because stability samples failed impurity tests.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur PSA Assay kits to emphasize that PSA values must be interpreted according to current clinical guidelines for biochemical recurrence.
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Mentor Texas, LP. is recalling 65 units of MENTOR CPX4 breast tissue expanders because a 350cc unit was found in a carton intended for 450cc units.
Amerisource Health Services is recalling 221 cartons of mixed amphetamine tablets due to unit dose mispackaging, where blister cavities may contain more than one tablet.
Teva North America is voluntarily recalling 1,299 bags of Argatroban Injection due to Current Good Manufacturing Practice (CGMP) deviations.