State

Tennessee product recalls

73,824 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,860
Critical: 1,324
Severe: 1,974
Most recent: 2026-11-04

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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48301–48325 of 81684

CriticalFDA (Food)·F-1896-2017·2017-05-03
Deutsch Kase Haus Recalls Semi-Soft Cheese for Listeria Risk
Deutsch Kase Haus, LLC is recalling specific lots of semi-soft cheese due to potential Listeria monocytogenes contamination. The affected products were distributed to multiple states.
Product
Semi Soft cheese with yogurt cultures and with or without vegetables. All affected product private labeled for other companies. Brands: Guggisberg; Product packaged as: 6lb deli horns (4 diameter x 13 long cylinder) 2 per case; Products package in clear plastic…
Category
Food
Distribution
11 states
SevereFDA (Drugs)·D-0687-2017·2017-05-03
Isomeric Pharmacy Recalls Phenylephrine and Tropicamide Ophthalmic Drops
Isomeric Pharmacy Solution, LLC is recalling 5,165 bottles of Phenylephrine 2.5% and Tropicamide 1% ophthalmic drops due to a lack of assurance of sterility.
Product
Phenylephrine 2.5%, Tropicamide 1%, 15 mL Multi-Dose Ophthalmic (spelled Opthalmic) Drops in a bottle, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1300, barcode 3 70285 13001 4.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0683-2017·2017-05-03
Isomeric Pharmacy Recalls Triamcinolone Acetonide Injection Vials for Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 2,335 vials of Triamcinolone Acetonide and Lidocaine HCl injection due to production processes that cannot assure sterility.
Product
Triamcinolone Acetonide 40 mg/mL, Lidocaine HCl 10 mg/mL , 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1020, barcode 3 70285 10201 1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0677-2017·2017-05-03
FDA Recalls Unapproved hCG Body Shaper Product for Contamination
The FDA is recalling hCG Body Shaper because it was marketed without approval and contains human chorionic gonadotropin, making it an unapproved drug.
Product
hCG Body Shaper, Highly Purified Human Chorionic Gonadotrophin 5000 IU, Colloidal Silver B12, Stabilizers/Excipients, Not For Medical Use, Must Be Refrigerated, Distributed by HCG Body Shaper, St. Peters, MO
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1832-2017·2017-05-03
HeartWare HVAD Pump Driveline Splice Kit Recall for Improved Repair
Medtronic is notifying clinicians that an improved splice kit is available to replace the HeartWare HVAD Pump Driveline Splice Kit due to a safety issue.
Product
HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product Usage: Is intended to repair the driveline cable once an electrical break has been identified. These repairs are limited to the portion of the driveline that is outside the patient boundary (exit…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V297000·2017-05-03
Audi Recalls 2017 Q5 Vehicles Due to Gearbox Defect
Volkswagen Group of America is recalling 2017 Audi Q5 vehicles because a gearbox defect may allow the vehicle to roll unexpectedly while in Park.
Product
AUDI — AUDI Q5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V289000·2017-05-03
Porsche Recalls Macan Models Due to Fuel Pump Flange Crack Risk
Porsche is recalling 2015-2017 Macan models because a fuel pump flange may crack, causing a fuel leak that increases fire risk.
Product
PORSCHE — PORSCHE MACAN S, MACAN TURBO, MACAN, MACAN GTS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0682-2017·2017-05-03
Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 2,352 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.
Product
Methylprednisolone Acetate 80 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1011, barcode 3 70285 10111 3.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1538-2017·2017-05-03
Heartware Recalls HVAD System Controllers for Exchange
Heartware is recalling all HVAD System Controllers currently on the market to exchange them for the next generation HVAD Controller (Controller 2.0).
Product
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare Ventricular Assist System…
Category
Medical Device
Distribution
37 states
SevereFDA (Food)·F-1893-2017·2017-05-03
Pepper Colby-Jack Cheese Recalled for Potential Listeria Contamination
Deutsch Kase Haus, LLC is recalling various brands of pepper cheese due to potential Listeria monocytogenes contamination. The product was distributed across 11 states.
Product
Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; Thunder Jack; Firecracker; Jalapeno Jack; Jumping Jack) cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Amish Classics; Lipari Old Tyme; Walnut Creek…
Category
Food
Distribution
11 states
SevereFDA (Drugs)·D-0686-2017·2017-05-03
Isomeric Pharmacy Recalls Testosterone Injection Vials Due to Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 2,156 vials of Testosterone Cypionate and Propionate injection due to production processes that cannot assure sterility.
Product
Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V298000·2017-05-03
Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Crack Risk
Volkswagen Group of America is recalling 2013-2017 Audi Q5 and Q7 vehicles because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.
Product
AUDI — AUDI Q5, Q7
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0685-2017·2017-05-03
Isomeric Pharmacy Recalls Injection Vials Due to Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 851 vials of a multi-dose injection product because production processes cannot assure sterility.
Product
Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1101, barcode 3 70285 11013 9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0681-2017·2017-05-03
Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 4,001 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.
Product
Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1010, barcode 3 70285 10101 4.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-2095-2017·2017-05-03
ConAgra Recalls Premium Hunt's Chili Kits for Potential Salmonella
ConAgra Foods is recalling Premium Hunt's Chili Kits due to potential Salmonella contamination in the spice packets. The recall covers 5,458 cases distributed nationwide.
Product
Premium Hunt's Chili Kit, Total NET WT 44.8 OZ (2.80 LB) 1.27kg; Directions: 1) Cook and stir meat in saucepan over medium-high 7 minutes or until done; drain. 2) Stir in all remaining ingredients; simmer 10 minutes, stirring occasionally. Con Agra Foods, P.O BOX 3768, Dept.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1888-2017·2017-05-03
Remel Blood Agar Plates Recalled for Listeria Contamination
Remel Inc is recalling Blood Agar plates due to confirmed surface contamination with Listeria monocytogenes. The products were distributed nationwide and in Puerto Rico.
Product
Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood Agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1877-2017·2017-05-03
Cardiovascular Systems Recalls ViperWire Advance Guide Wires Due to Packaging Error
Cardiovascular Systems Inc is recalling 595 units of ViperWire Advance guide wires because 0.018-inch products were packaged as 0.014-inch.
Product
ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14. Product Usage: The Stealth 360 Orbital PAD System and the Diamondback 360 Peripheral Orbital Atherectomy System are percutaneous orbital atherectomy systems…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1878-2017·2017-05-03
Ulrich Medical Recalls uNion Cervical Plate System for Screw Mechanism Defect
Ulrich Medical USA Inc is recalling 4,854 uNion Cervical Plate Systems because static plate screws may disassociate. The recall covers devices distributed in 20 US states.
Product
uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the cervical spine (C2 to Ti). The system is to be used to provide stabilization of the anterior cervical spine as an adjunct to fusion for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0684-2017·2017-05-03
Isomeric Pharmacy Recalls Triamcinolone Diacetate Vials Due to Sterility Concerns
Isomeric Pharmacy Solution, LLC is recalling 1,951 vials of Triamcinolone Diacetate injection because production processes cannot assure sterility. The FDA has classified this as a Class II recall.
Product
Triamcinolone Diacetate 40 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1021, barcode 3 70285 10211 0.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1889-2017·2017-05-03
Merit Medical Recalls 1 mL Medallion Syringes Due to Plunger Tip Defect
Merit Medical Systems is voluntarily recalling 1 mL Medallion Syringes because of a defect in the syringe plunger tip.
Product
1 mL Medallion¿ Syringe. Catalog Numbers: 701989001, K01-05197P, MSS011-YP, K01-07946P, MSS011, MSS011-LB, MSS011-R, MSS011-Y, MSS011P, MSS011-LBP, MSS011-DG, K08-02926AP, K01-07742P, K10-05457P.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1884-2017·2017-05-03
XTANT Medical Recalls 5.5mm CoCr Straight Rods Due to Labeling Error
XTANT Medical Inc. is recalling 97 units of 5.5mm CoCr Straight Rods because the labels may incorrectly identify the material as Ti6Al-4V ELI instead of Cobalt Chromium.
Product
5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one piece per bag. Product Usage: The 5.5mm dia. X 500 mm CoCr Straight Rod is an accessory to the Fortex Pedicle Screw System. It is a straight rod connected…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0679-2017·2017-05-03
Novartis Recalls Pilocarpine Hydrochloride Ophthalmic Solution for Impurity Failures
Novartis Pharmaceuticals Corp. is recalling Pilocarpine Hydrochloride Ophthalmic Solution 4% due to failed impurities and degradation specifications.
Product
PILOCARPINE HYDROCHLORIDE — PILOCARPINE HYDROCHLORIDE (PILOCARPINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1875-2017·2017-05-03
Siemens ACUSON S Family Ultrasound Systems Recalled for Image Display Defects
Siemens is recalling 2,045 ACUSON S Family ultrasound systems because the 18L6 HD transducer may display a triple image or a dark band, potentially affecting diagnostic accuracy.
Product
18L6 HD transducer on the ACUSON S Family ultrasound systems with software versions VD10A or VD10C; Model numbers: 18L6 HD transducer 10041227 & 10789400 S1000 10441701 S2000 10041461 S2000 (Refurb) - 10440017 S3000 10441730 Radiology: The ultrasound imaging…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0678-2017·2017-05-03
Novartis Recalls Isopto Carpine Eye Drops for Impurity Failures
Novartis Pharmaceuticals is recalling specific lots of Isopto Carpine eye drops due to failed impurities and degradation specifications.
Product
Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4%, packaged in 15 mL bottle, Rx only, Manufactured by: Alcon Laboratories, Inc. Fort Worth Texas 76134 USA NDC 0998-0206-15
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1876-2017·2017-05-03
Becton Dickinson Recalls Trypticase Soy Agar and Chocolate Agar I-Plates
Becton Dickinson is recalling one lot of Trypticase Soy Agar and Chocolate Agar I-Plates because they may fail to recover specific Haemophilus organisms.
Product
BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) and Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX) I Plate Product Usage: Testing - Trypticase Soy Agar with 5% Sheep Blood is used for the growth of fastidious organisms and for the visualization of…
Category
Medical Device
Distribution
Distributed nationwide