State

Tennessee product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47126–47150 of 81677

HighFDA (Devices)·Z-2685-2017·2017-07-12
PerkinElmer Multiphor II Electrophoresis System Recalled for Electric Shock Risk
PerkinElmer is recalling 241 Multiphor II Electrophoresis Systems due to a potential electric shock hazard if grommets are not installed.
Product
Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2656-2017·2017-07-12
JAS Diagnostics Recalls Drew Scientific DREW 3-PAC Reagent Kits
JAS Diagnostics Inc. is recalling 14,064 units of Drew Scientific DREW 3-PAC Reagent Kits because they may result in elevated platelet backgrounds during routine startup checks.
Product
Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-2672-2017·2017-07-12
Ion Beam Applications Recalls Proteus Proton Therapy Systems for Software Issues
Ion Beam Applications is recalling Proteus 235 and Proteus ONE proton therapy systems because on-site software installations were not performed consistently with standard operating procedures.
Product
Proteus 235 and Proteus ONE proton therapy systems
Category
Medical Device
Distribution
10 states
ModerateFDA (Devices)·Z-2658-2017·2017-07-12
Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-packaging Error
Encore Medical is recalling 9 units of 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.
Product
3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2665-2017·2017-07-12
Exactech Equinoxe Modular Reverse Pilot-Tip Starter Reamer Recall
Exactech is recalling 928 Equinoxe Modular Reverse Pilot-Tip Starter Reamers to update instructions for use. The update clarifies proper reaming technique to prevent instrument breakage.
Product
EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #: 321-25-01
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2664-2017·2017-07-12
Exactech Equinoxe Glenoid Reamer Recalled for Updated Instructions
Exactech is recalling Equinoxe Glenoid Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38, Catalog #: 321-05-42, and Catalog #: 321-05-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2668-2017·2017-07-12
Exactech Equinoxe Reamer Recall Due to Updated Instructions for Use
Exactech is recalling Equinoxe Narrow Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #: 321-45-38, Catalog #: 321-45-42 and Catalog #: 321-45-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2663-2017·2017-07-12
Exactech Equinoxe Reverse Starter Reamer Recalled for Updated Instructions
Exactech is recalling 382 Equinoxe Reverse Starter Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2662-2017·2017-07-12
Exactech Recalls Logic Fit Tibial Tamp Heads for Labeling Clarification
Exactech, Inc. is recalling 573 Logic Fit Tibial Tamp Heads to update surgical labeling. The update clarifies proper removal techniques to prevent instrument breakage.
Product
Logic Fit Tibial Tamp Head
Category
Medical Device
Distribution
32 states
ModerateFDA (Devices)·Z-2669-2017·2017-07-12
Sterilmed Recalls Reprocessed EP Ablation Cables Due to Regulatory Status
Sterilmed is recalling 963 reprocessed EP ablation cables because they are Class III devices that lack required premarket approval.
Product
Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the appropriate number of tails on the proximal end. The cables serve two different purposes. They either serve as an extension between an EP catheter and…
Category
Medical Device
Distribution
17 states
ModerateFDA (Drugs)·D-0945-2017·2017-07-12
G & W Clobetasol Propionate Ointment Recalled for Impurity
G & W Laboratories is recalling Clobetasol Propionate Ointment 0.05% due to out-of-specification results for a known impurity.
Product
CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0937-2017·2017-07-12
Methocarbamol USP Recalled for Quality Assurance Deviations
American Pharmaceutical Ingredients LLC is recalling Methocarbamol USP due to lack of quality assurance at the API manufacturer.
Product
Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC: 58597-8023-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2660-2017·2017-07-12
Leica ASP6025 Tissue Processor Recalled for Incorrect Voltage Labeling
Leica Microsystems is recalling 812 ASP6025 Tissue Processors because the voltage labels on the rear alarm connectors are incorrect.
Product
Nussloch GmbH ASP6025 Tissue Processor
Category
Medical Device
Distribution
36 states
ModerateFDA (Devices)·Z-2666-2017·2017-07-12
Exactech Equinoxe Modular Reverse Pilot-Tip Reamer Recall for Labeling Clarification
Exactech is recalling Equinoxe Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer, Catalog #: 321-25-38, Catalog #: 321-25-42 and Catalog #: 321-25-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Drugs)·D-0944-2017·2017-07-12
GSK Recalls Parodontax Toothpaste Due to Possible Metal Presence
GSK Consumer Healthcare is recalling 15,708 tubes of Parodontax Whitening toothpaste due to the possibility of metal in the product.
Product
PARODONTAX — PARODONTAX (STANNOUS FLUORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0934-2017·2017-07-12
PharMEDium Recalls Ropivacaine HCl Injection Due to Labeling Errors
PharMEDium Services, LLC is recalling 21 pumps of Ropivacaine HCl 0.2% injection due to incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0935-2017·2017-07-12
PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling
PharMEDium Services is recalling two Bupivacaine HCl ON-Q pumps due to incorrect or missing lot and expiration date labeling.
Product
Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2659-2017·2017-07-12
Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-Packaging
Encore Medical is recalling 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.
Product
3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0932-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors
PharMEDium Services is recalling 147 Ropivacaine HCl IV pumps nationwide because of incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0930-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Labeling
PharMEDium Services is recalling 79 Ropivacaine HCl IV pumps because of incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-256-09
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0936-2017·2017-07-12
PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling
PharMEDium Services is recalling seven Bupivacaine HCl ON-Q pumps because of incorrect or missing lot and expiration dates.
Product
Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-023-09
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0931-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors
PharMEDium Services is recalling 22 Ropivacaine HCl pumps nationwide because of incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-03
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0933-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Lot and Expiration Dates
PharMEDium Services, LLC is recalling 10 Ropivacaine HCl 0.2% ON-Q pumps nationwide due to incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 600 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-279-33
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V465000·2017-07-11
Kawasaki Recalls 2017 Versys 650 Motorcycles for Loose Tail Light Socket
Kawasaki is recalling 2017 Versys 650 motorcycles because a loose tail/brake light socket may allow the bulb to fall out, increasing crash risk.
Product
KAWASAKI — KAWASAKI VERSYS 650
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17754·2017-07-11
Superpedestrian Recalls Electric Bicycle Conversion Wheels Due to Axle Failure
Superpedestrian is recalling about 230 Copenhagen electric bicycle conversion wheels because the rear axle can fail, posing fall and crash hazards to riders.
Product
Electric bicycle conversion Copenhagen wheels
Category
Consumer Product
Distribution
Distributed nationwide