State
72,913 recalls have nationwide distribution and so reach Tennessee. 7,819 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,819 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 7,819 recalls whose distribution notice names Tennessee specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Halyard Drape Packs, kit code LMDP36-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 72 kits affected.
CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.
Merlin Patient Care System programmer software is being recalled because a malfunction during a pacing capture threshold test may stop the command to terminate the test being communicated.
Three lots of the Siemens Dimension Tacrolimus Flex reagent cartridge are being recalled because of a potential positive bias in quality control and patient sample results.
Halyard Eye Bag Packs, kit code UIEB48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 60 kits affected.
MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PUSH OTW, catalog number 8170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Halyard Pain Packs, kit code AMPK48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 120 kits affected.
CGuard Prime Carotid Stent Systems, 135 cm with a 9 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
CORFLO Safety PEG Kits, catalog number 30-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 231 kits are affected.
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
Park St. Deli Macaroni & Cheese, 20 oz, is being recalled because of undeclared soy lecithin. The action covers 58,405 cases.
CGuard Prime Carotid Stent Systems, 135 cm with a 9 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Hintermann Series Talar Implants, Left, Size 2, are being recalled because packaging and labeling for a left implant contained a right implant device. 67 units are affected.
Primidone Tablets, USP, 50 mg, from Amneal are being recalled over the potential for cross-contamination with acemetacin API due to an issue at the API manufacturer. 27,936 bottles affected.
Epinephrine Injection, USP, 1 mg/mL single-dose vials from Fresenius Kabi are being recalled because they failed impurities and degradation specifications. 898,050 vials affected.
The SporeTraq Mail-In Spore Testing Service, 52 tests, is being recalled because an incorrect incubation process was performed on the product. 2,210 units are affected.
The SporeTraq Mail-In Spore Testing Service, 12 tests, is being recalled because an incorrect incubation process was performed on the product.
Boston Scientific CSK stainless steel electrodes across several lengths are being recalled because the reusable electrodes may not meet expected performance levels. 31,923 units affected.
Neuro Nourish, a 6-in-1 nutritional supplement, is being recalled because premature lipid oxidation may give the product an off odor and bitter taste. 512 units affected.
Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, are being recalled after an out-of-specification dissolution result at the ninth month of testing. 360 bottles affected.
EXCOR Pediatric VAD System blood pump PU valves are being recalled because the inner package expiration date does not match the correct outer package date.
Boston Scientific TCN nitinol electrodes across four lengths are being recalled because the reusable electrodes may not meet expected performance levels. 49,251 units affected.