State

Tennessee product recalls

72,986 recalls have nationwide distribution and so reach Tennessee. 7,821 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,821
Critical: 1,317
Severe: 1,653
Most recent: 2026-09-16

Of the 7,821 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 7,821 recalls whose distribution notice names Tennessee specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6801–6825 of 80807

SevereFDA (Devices)·Z-1760-2025·2025-05-28
Centerline Biomedical IOPS Guidewire 2 Coating Delamination Risk
Centerline Biomedical is recalling the IOPS Guidewire 2 (Lot 2404-2005) because the coating may delaminate during use, potentially compromising the guidewire's function during catheter placement procedures.
Product
Centerline Biomedical IOPS Guidewire 2, REF ATW-2; Sensorized wire used to navigate through vasculature to facilitate placement of a catheter
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-1807-2025·2025-05-28
TRUE 3D VIEWER SYSTEM displays medical images with incorrect orientation
Echopixel's TRUE 3D VIEWER SYSTEM may display imaging data with incorrect orientation (left/right/superior/inferior/anterior/posterior), which could lead to inaccurate measurements during clinical use.
Product
TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0, 1.25, and 1.35 The t3D-Viewer is designed for use by health care professionals HCPs and is intended to assist the clinician who is responsible for making all patient management decisions. The True 3D V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0444-2025·2025-05-28
AIRSUPRA Albuterol and Budesonide Inhalation Aerosol Recalled for Defective Delivery System
AstraZeneca is recalling AIRSUPRA (albuterol sulfate and budesonide) inhalation aerosol due to a defective delivery system. The recall affects multiple lot numbers and expiration dates distributed nationwide.
Product
AIRSUPRA — AIRSUPRA (ALBUTEROL SULFATE AND BUDESONIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1805-2025·2025-05-28
Philips MR 7700 Medical Device Alignment Error in MobiView Application
Philips is recalling MR 7700 model medical devices due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1789-2025·2025-05-28
SmartPath to dStream 3.0T Medical Device Recall for Software Error
Philips is recalling the SmartPath to dStream 3.0T medical device due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. This could affect image interpretation accuracy.
Product
Product Name: SmartPath to dStream for 3.0T; Model Number: 782145
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2025·2025-05-28
Philips Ingenia Ambition X MRI Systems Alignment Error in MobiView
Philips is recalling certain Ingenia Ambition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1787-2025·2025-05-28
Check-Flo Performer Introducer Medical Device Recall Notice
Cook Incorporated is recalling Check-Flo Performer Introducer devices because some units from affected lots may contain an incorrectly sized introducer sheath.
Product
Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN) REF RCFW-14.0-0-38-30-RB, Order Number (GPN) REF G08957,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1791-2025·2025-05-28
SmartPath to Ingenia Elition X MRI Systems Alignment Error Recall
Philips is recalling SmartPath to Ingenia Elition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The alignment errors could affect image interpretation.
Product
Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0806-2025·2025-05-28
Yellowstone Brown Sugar Molasses Baked Beans Recall for Undeclared Soy
Vietti Acquisitions, LLC is recalling Yellowstone Brown Sugar Molasses Baked Beans because the cans are mislabeled and actually contain Beef and BBQ Baked Beans with undeclared soy, a common allergen.
Product
Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in cans, packed 12 cans per case. UPC: 071846187071; Packaged by: Vietti Foods Inc. Nashville, TN 37203
Category
Food
Distribution
23 states
HighNHTSA·25V352000·2025-05-28
Mack Recalls 2026 Granite Trucks Due to Incorrect Brake Drum Load Ratings
Mack Trucks is recalling 2026 Granite trucks because incorrect drive axle brake drums were installed, leading to inaccurate weight rating information on the door jamb label.
Product
MACK — MACK GRANITE GR (4)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1812-2025·2025-05-28
PhenoMATRIX bacterial culture plate interpretation software recalled nationwide
Copan WASP is recalling PhenoMATRIX, an AI-powered bacterial culture plate interpretation software, because it lacks required FDA premarket approval, creating potential risk of inaccurate colony counts and morphology data that could affect patient diagnosis.
Product
PhenoMATRIX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0807-2025·2025-05-28
Lactoferrin Apolactoferrin Vegetarian Capsules Recalled for Undeclared Milk
My Life Inc is recalling Lactoferrin as Apolactoferrin 300 mg vegetarian capsules (UPC 8 50062 61315 7) because they contain undeclared milk allergen, which poses a risk to consumers with milk allergies.
Product
Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg per serving. UPC 8 50062 61315 7. Amazon ASIN #B0DNLMBHGG.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1808-2025·2025-05-28
BD Cathena Safety IV Catheter manufacturing defect hole septum
Becton Dickinson is recalling certain BD Cathena Safety IV Catheter models due to a manufacturing defect that may create a hole in the septum, potentially causing blood leakage during insertion.
Product
BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter 20GX1.00IN STRAIGHT BC, REF: 386803; BD Cathena Safety IV Catheter BD Multiguard Technology 20 GA x 1.00 IN, 386862
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1785-2025·2025-05-28
True 3D Viewer Model EP-00003 Software Orientation Display Issue Recall
Echopixel's True 3D Viewer (Model EP-00003) with certain software versions can display ultrasound image orientation incorrectly, potentially leading to misdiagnosis or incorrect surgical planning.
Product
True 3D Viewer, Model: EP-00003
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0446-2025·2025-05-28
Phentermine Hydrochloride Capsules 30mg Recalled for cGMP Deviations
KVK Tech, Inc. is recalling 9,680 bottles of Phentermine Hydrochloride Capsules 30mg nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall is voluntary and firm-initiated.
Product
PHENTERMINE HYDROCHLORIDE — PHENTERMINE HYDROCHLORIDE (PHENTERMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1788-2025·2025-05-28
Philips SmartPath to dStream 1.5T medical device alignment recall
Philips is recalling certain SmartPath to dStream 1.5T medical imaging devices due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1795-2025·2025-05-28
Ingenia 1.5T MRI Systems Recalled for Alignment Errors
Philips is recalling Ingenia 1.5T MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1793-2025·2025-05-28
Evolution Upgrade 1.5T imaging system alignment error recall
Philips Evolution Upgrade 1.5T medical imaging systems may display alignment errors in cross-reference line functionality when reviewing images via MobiView application.
Product
Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1792-2025·2025-05-28
Philips Upgrade to MR 7700 Medical Device Alignment Error Recall
Philips is recalling the Upgrade to MR 7700 (Model 782130) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The misalignment could affect diagnostic accuracy.
Product
Product Name: Upgrade to MR 7700; Model Number: 782130;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1813-2025·2025-05-28
HiResolution Bionic Ear System M Battery Charger Labeling Mismatch Recall
Advanced Bionics, LLC is recalling six units of the HiResolution Bionic Ear System - M Battery Charger (Model CI-5607) due to incorrect product labeling that does not match the intended product.
Product
HiResolution" Bionic Ear System - M Battery Charger Model Number CI-5607
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-1799-2025·2025-05-28
Philips Ingenia 1.5T CX MRI System Alignment Error Potential
Philips is recalling Ingenia 1.5T CX MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application. This could affect image interpretation.
Product
Product Name: Ingenia 1.5T CX; Model Number: 781262;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1806-2025·2025-05-28
Smith & Nephew Lag/Compression Screw Kit Undersized Socket Defect
Smith & Nephew is recalling a Lag/Compression Screw Kit (REF: 71642690) because some compression screws have undersized hexagon sockets that render them non-functional and require replacement.
Product
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1794-2025·2025-05-28
Philips Evolution Upgrade 3.0T MRI Cross Reference Line Alignment Error
Philips is recalling Evolution Upgrade 3.0T MRI systems (Models 782117 and 782143) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0443-2025·2025-05-28
Esomeprazole Magnesium oral suspension recalled for failed impurity specifications
Zydus Pharmaceuticals is recalling Esomeprazole Magnesium delayed-release oral suspension, 20 mg, due to out-of-specification test results for unknown degradation products detected during long-term stability testing.
Product
ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1790-2025·2025-05-28
Philips SmartPath to dStream Medical Imaging Software Alignment Error
Philips is recalling SmartPath to dStream for XR and 3.0T medical imaging software due to potential alignment errors in cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113;
Category
Medical Device
Distribution
Distributed nationwide