State

Tennessee product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51051–51075 of 81687

SevereFDA (Devices)·Z-0119-2017·2016-10-26
Synergetics VersaVit 2.0 Procedure Packs Recalled for Pressure Defect
Synergetics Inc is recalling 72 units of 25 gauge VersaVit 2.0 Core Essentials Procedure Packs because the vitrectomy cutters do not operate within correct pressure pulse specifications.
Product
25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E, packaged in HIPS rigid tray with a Tyvek lid sterile barrier system.
Category
Medical Device
Distribution
14 states
SevereFDA (Food)·F-0177-2017·2016-10-26
Dollar General Recalls Mold-Contaminated Soft Baked Chocolate Brownie Cookies
Dollar General is recalling Soft Baked Chocolate Brownie Cookies due to the presence of mold. Consumers should discard the product or return it for a refund.
Product
Cookies Bergen, Soft Baked Chocolate Brownie Cookies, NET WEIGHT: 4.44 OZ (126g), Produced by P.W. Sponmet Sp.l., Poland
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0231-2017·2016-10-26
Windstone Medical Recalls Major General Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 852 Major General Packs because Medtronic gloves inside may have splits or holes that compromise sterility.
Product
Major General Pack, Kit number 002645-11 and 002645-12 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0260-2017·2016-10-26
Windstone Medical Packaging Recalls Peri Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 115 Peri Kits (PSS1037) because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Peri Kit, Kit number PSS1037 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0054-2017·2016-10-26
Vascular Solutions Recalls Twin-Pass RX Dual Access Catheters Due to Manufacturing Defect
Vascular Solutions is recalling Twin-Pass RX Dual Access Catheters because excess manufacturing material may remain at the tip or within the distal lumen.
Product
Vascular Solutions Twin-Pass RX Dual Access Catheter, model 5210. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200 and 5230)…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V780000·2016-10-26
Forest River Recalls 2016 Rockport Trucks Due to Fuel Pressure Loss Risk
Forest River is recalling 2016 Rockport cargo and work trucks because the rear ramp may damage fuel connections, causing engine stalls and crash risk.
Product
FOREST RIVER — FOREST RIVER ROCKPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0141-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility in custom surgical kits.
Product
Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0274-2017·2016-10-26
Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that compromise sterility.
Product
Taymour GYN Pack, Kit number PSS2642 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0053-2017·2016-10-26
Vascular Solutions Recalls Twin-Pass Catheters Due to Manufacturing Material
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the tip or in the distal lumen.
Product
Vascular Solutions Twin-Pass Dual Access Catheter, models 5200, 5210, and 5230. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0105-2017·2016-10-26
Arbor Pharmaceuticals Recalls Cetylev Tablets Due to Defective Blister Packaging
Arbor Pharmaceuticals is recalling Cetylev (acetylcysteine) effervescent tablets because incomplete seals on the blister packaging allow moisture to enter, causing the tablets to swell.
Product
Cetylev (acetylcysteine) effervescent tablets for oral solution, 500 mg, Rx Only, 20 tablets per carton (ten 2 count blister packs), Distributed by Arbor Pharmaceuticals, LLC Atlanta, GA 30328, NDC 24338-700-10.
Category
Drug
Distribution
14 states
SevereNHTSA·16V777000·2016-10-26
Ford Recalls 2010-2012 Escape and 2010-2011 Mariner for Fuel Leak Risk
Ford is recalling specific 2010-2012 Escape and 2010-2011 Mariner vehicles because a cracked fuel delivery module may cause a fuel leak, increasing the risk of fire.
Product
FORD — FORD, MERCURY ESCAPE, MARINER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0212-2017·2016-10-26
Del Monte Recalls Cut Green Beans Due to Crawfish Parts
Del Monte is recalling cut green beans and field peas with snaps due to a customer complaint of finding crawfish parts in the product.
Product
Cut Green Beans packed under brand names of: Allens Cut Green Beans (Ejotes Cortados Lago Azul) Blue Lake . Allens Cracker Barrel Label (Both labels have same UPC # - different sodium content - 140 mg for Allens Cut Green Beans and 250 for Cracker Barrel label Peso Neto…
Category
Food
Distribution
22 states
SevereFDA (Devices)·Z-0005-2017·2016-10-26
Heartware Ventricular Assist System Controller Recall for Loose Connector Ports
Heartware, Inc. is recalling Ventricular Assist System Controllers due to loose connector ports. The recall affects 4,235 units worldwide, including 7,272 in the U.S.
Product
HeartWare Ventricular Assist System Controller Product Usage: 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 HVAD is designed for in-hospital and out-of-hospital settings…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0213-2017·2016-10-26
Del Monte Recalls Field Peas and Green Beans Due to Crawfish Parts
Del Monte is recalling approximately 15,000 cases of canned field peas and green beans after a customer complaint reported finding crawfish parts in the product.
Product
Allens East Texas Fair Brand, Tiny Tender Field Peas with snaps; NET.WT. 6 lbs. 15 oz.. (3.15kg) UPC 0 34700 623214 8 Distributed by Sager Creek Vegetable Company, Siloam Springs, AR 72761-0250 USA; UPC 0 34700 63213 1
Category
Food
Distribution
22 states
SevereFDA (Devices)·Z-0055-2017·2016-10-26
Vascular Solutions Recalls Twin-Pass Dual Access Catheters Due to Manufacturing Residue
Vascular Solutions is recalling Twin-Pass dual access catheters because excess manufacturing material may remain at the catheter tip or within the distal rapid exchange lumen.
Product
Vascular Solutions Twin-Pass .023" Dual Access Catheter, model 5230. Sterilized with Ethylene Oxide. The Twin-Pass dual access catheter is a dual lumen catheter designed for use in the coronary and/or peripheral vasculature. The Twin-Pass catheter (Models 5200 and 5230)…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V778000·2016-10-26
Ford Recalls 2017 F-Series Trucks Due to Fuel Leak Fire Risk
Ford is recalling 2017 F-250 through F-550 Super Duty trucks because a fuel shield may detach, causing a leak that increases fire risk.
Product
FORD — FORD F-550 SD, F-350 SD, F-450 SD, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0044-2017·2016-10-26
Teleflex Medical Recalls Willy Rusch Tracheostomy Tube Sets
Teleflex Medical is recalling Willy Rusch Tracheostomy Tube Sets because the connector may disconnect from the tube during use.
Product
Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow tracheostoma and narrow-lumen tracheas. When using cannulas with curr. For short term intermittent inflation.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0180-2017·2016-10-26
Windstone Medical Packaging Recalls Endoscopy Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 304 Endoscopy Packs because disposable gloves in the kits may have splits or holes that compromise sterility.
Product
Endoscopy Pack, Kit number PSS1646 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0290-2017·2016-10-26
RTI Surgical Recalls Streamline OCT Spinal Rods Due to Cracks
RTI Surgical is voluntarily recalling 66 units of Streamline OCT spinal rods due to potential cracks that could reduce strength and cause patient injury.
Product
RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Product Usage: When intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (occiput-T3), the Streamline OCT Occipito-Cervico-Thoracic System is…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0118-2017·2016-10-26
Awareness Boost Tea Recalled for Potential Salmonella Contamination
Awareness Corporation is recalling 2,697 bottles of Boost Tea dietary supplement due to potential Salmonella contamination. The product was distributed in 34 U.S. states and D.C.
Product
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness Corporation P.O. Box 2289 Chandler, AZ 85244
Category
Food
Distribution
33 states
SevereFDA (Devices)·Z-0185-2017·2016-10-26
Windstone Medical Packaging Recalls Extremity Tray Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 816 Extremity Tray kits because the included Medtronic gloves may have splits or holes that compromise sterility.
Product
Extremity Tray, Kit number AMS1200(B and AMS1200(C convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0233-2017·2016-10-26
Windstone Medical Packaging Recalls Major Laparotomy Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 12 Major Laparotomy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Major Laparotomy Pack - NS, kit number AMS4347 convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0146-2017·2016-10-26
Fresh Express American Salad Recalled for Incorrect Condiment Kits
Fresh Express is recalling American Salad bags that may contain incorrect condiment kits. Consumers in six states should check their products.
Product
Fresh Express American Salad, 11 oz., Product Code G264A12B, Use-By Date OCT 05
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-0263-2017·2016-10-26
Windstone Medical Recalls Plastic Packs with Defective Gloves
Windstone Medical Packaging is recalling 204 plastic packs used in general surgery because the included Medtronic gloves may contain splits or holes that compromise sterility.
Product
Plastic Pack , Kit number AMS1833(A convenience custom kits used for general surgery in hospital operating room
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0124-2017·2016-10-26
Kabobs Recalls Mini Cheese Quiche Due to E. coli O121 Contamination
Kabobs Inc is recalling 377 cases of Mini Cheese Quiche because the flour used was contaminated with E. coli O121. The product was distributed across 28 states.
Product
MINI CHEESE QUICHE, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Category
Food
Distribution
27 states