State
73,833 recalls have nationwide distribution and so reach Tennessee. 7,861 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,861 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 7,861 recalls whose distribution notice names Tennessee specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hartley Medical Center Pharmacy is recalling Baclofen 2000 mcg/ml syringes because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine HCL syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling two syringes of Morphine Sulfate 1.5 mg/ml due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 10 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Arrow International is recalling specific Percutaneous Insertion Trays because the sheath body may separate from the hub, posing a risk of bleeding.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 2 mg/ml syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Sufentanil Citrate/Clonidine/Bupivacaine syringes because the agency could not ensure the product was sterile.
Mack is recalling 2016-2017 Titan trucks because a steering shaft bolt may fail, causing loss of steering and potential crashes.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 20 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Ventura Foods LLC is recalling Land O Lakes margarine cups because they were distributed without labels, failing to disclose milk and soy allergens.
Gi Supply is recalling Large Volume Paracentesis Kits because the pinch clamp on the RP Bag may be missing, posing a splash hazard to users.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate, Sufentanil Citrate, and Bupivacaine HCL vials due to a lack of assurance of sterility.
Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.
Philips Respironics is recalling approximately 104,508 Trilogy and Garbin ventilators due to a software issue. The recall covers units distributed nationwide and internationally.
Sedecal S.A. is recalling 349 mobile X-ray systems because static electricity and other issues can cause uncommanded movements.
SRAM is recalling Zipp 88 aluminum front hubs because the flanges can fail, posing a crash and injury hazard. Consumers should stop using the hubs and contact SRAM for a free replacement.
Arrow International Inc. is recalling Super Arrow-Flex Percutaneous Sheath Introducer Sets because packaging damage may compromise sterility, posing a potential infection risk.
Terex is recalling 2015-2016 aerial devices and digger derrick lifts because the suspension circuit can inflate air bags, lifting outriggers and increasing injury risk.
SRAM is recalling Zipp bicycle quick releases because they may fail to engage, posing crash and injury hazards to riders.
Eastland Food Corporation is recalling Maesri Brand Shrimp Powder because it contains FD&C Yellow #6, which is not listed on the label.
Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.
GE Lighting is recalling high-intensity LED lamps because they can separate from their base and fall, posing an impact hazard. No injuries have been reported.
Biomet is recalling 21,268 Crosslock DVR ePAK surgical sets because components may oxidize during storage. This could cause an inflammatory reaction if material enters the surgical wound.
Spacelabs Healthcare is recalling Xhibit Central Station units because patient height and weight values may be switched, causing incorrect Body Surface Area calculations.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Calibrator E lots 42 and 43 because they show bias in the testosterone assay.