State

Tennessee product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42276–42300 of 81669

HighFDA (Devices)·Z-2242-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 2,396 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
3.2MM X 560MM COCR THD TIP; 14-441053 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2235-2018·2018-06-27
Zimmer Biomet Recalls Ball Tip Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 26 units of Ball Tip Guide Wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
BALL TIP GUIDE WIRE 2.0MMX60CM; 469020 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2232-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling trauma guide wires because packaging defects may allow sterile barrier breaches, creating a risk of infection.
Product
BALL TIP GUIDE WIRE 3.2MMX98CM; 469060 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2249-2018·2018-06-27
Vascular Solutions Recalls Drainer Centesis Catheters Due to Bacterial Endotoxins
Vascular Solutions, Inc. is recalling specific lots of Drainer Centesis Catheters because the supplier reported a potential for unsafe levels of bacterial endotoxins.
Product
Drainer(R) Centesis Catheters: (a) REF 8810, 5F x 9cm (b) REF 8811, 6F x 9cm (c) REF 8812, 5F x 15cm Product The Drainer centesis catheter is intended for use in percutaneous fluid aspirations and small volume drainage procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2256-2018·2018-06-27
Pentax C2 CryoBalloon Focal Catheter Recalled for Connector Alignment Defect
Pentax of America Inc is recalling 57 units of the C2 CryoBalloon Focal Catheter because a misaligned arrow may allow the catheter to detach from the controller during use.
Product
C2 CryoBalloon Focal Catheter, REF FG-1009. C2 CryoBalloon Ablation System is used as a cryosurgical tool in the field of general surgery, specifically for endoscopic applications.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2266-2018·2018-06-27
Datex-Ohmeda CARESCAPE R860 Ventilators Recalled for Display Processor Failure
Datex-Ohmeda is recalling CARESCAPE R860 ventilators with software version 10SP05 because the display processor may experience unexpected failure.
Product
CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The CARESCAPE R860 ventilator is designed to provide mechanical ventilation or support to neonatal, pediatric, and adult patients weighing 0.25 kg and above. The CARESCAPE R860 ventilator is a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2231-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
DRILL PT GUIDE WIRE 2MM X 60CM; 469320 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2233-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling specific trauma guide wires because packaging defects may allow sterile barrier breaches, creating a potential risk of infection.
Product
BALL TIP GUIDE WIRE 3.2MMX55CM; 469055 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V436000·2018-06-27
Forest River Recalls Salem and Wildwood Trailers Due to Shower Cover Defect
Forest River is recalling 2016-2019 Salem and Wildwood trailers because the outside shower cover may block the water heater exhaust, increasing injury risk.
Product
FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2237-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 832 trauma guide wires because packaging defects may compromise sterility, posing a risk of infection.
Product
G-PIN 2.8BL 3.2PL 98CM 2PK; 467260 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2255-2018·2018-06-27
Cyberonics VNS Therapy Programmer Model 3000 Recalled for Parameter Miscalculation
Cyberonics is recalling 252 VNS Therapy Programmer Model 3000 units because certain programming events can miscalculate parameters for implanted generators, potentially causing painful stimulation or lack of therapy.
Product
VNS Therapy Programmer, Model 3000, v1.0 System
Category
Medical Device
Distribution
21 states
HighFDA (Devices)·Z-2230-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
DRILL PT GUIDE WIRE 3.2MMX98CM, 469360 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2239-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Packaging Defects
Zimmer Biomet is recalling trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
BEAD TIP GD WIRE 3.0MM X 60CM; 29402 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2236-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 361 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
G-PIN 2.8BL 3.2PL 60CM 2PK; 467265 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2241-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 248 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
RECON DRILL 6MM X 439MM; 14-443023 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2243-2018·2018-06-27
C.R. Bard Recalls CritiCore Automated Urine Output and Temperature Monitor
C.R. Bard is recalling CritiCore Automated Urine Output and Temperature Monitors due to measurement errors and undesired alarms.
Product
CritiCore Automated Urine Output and Temperature Monitor
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-2240-2018·2018-06-27
Zimmer Biomet Recalls Trauma Guide Wires Due to Sterile Barrier Failure
Zimmer Biomet is recalling 304 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Product
3.2MM X 510MM COCR THD TIP; 14-443053 Intended to be used as a guide pin for insertion of implants (cannulated screws and/or intramedullary nails). Bone nail guidewire. Intended for drilling bone.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0886-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium tablets because they failed impurities and degradation specifications.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0888-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures
Dr. Reddy's Laboratories is recalling 130,081 bottles of Atorvastatin Calcium 40 mg tablets nationwide due to failed impurity and degradation specifications.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2270-2018·2018-06-27
Olympus JF-160F Duodenoscopes Recalled for New Reprocessing Procedures
Olympus Corporation of the Americas is recalling 68 JF-160F duodenoscopes nationwide to implement validated new reprocessing procedures.
Product
Olympus JF-160F duodenoscopes (Model NumberJF-160F)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0878-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Foreign Object
Dr. Reddy's Laboratories is recalling 6,397 bottles of Atorvastatin Calcium 80 mg tablets because a foreign object was found embedded in a tablet.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2261-2018·2018-06-27
Paragon 28 Recalls P28 JAWS Nitinol Staple Kits Due to Missing Drill Guide
Paragon 28, Inc. is recalling P28 JAWS Nitinol Staple System kits because the drill guide is missing from the package.
Product
P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones and joints of the foot including fixation of small bone fragments.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2267-2018·2018-06-27
Smith & Nephew Recalls Birmingham Hip Resurfacing Femoral Heads for Labeling Defects
Smith & Nephew is recalling two Birmingham Hip Resurfacing Femoral Heads because they were distributed in the US with non-US labeling.
Product
Birmingham Hip Resurfacing Femoral Head: (a) Size 58 mm, REF 74121158 (b) Size 56 mm, REF 74123156
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-2268-2018·2018-06-27
Smith & Nephew Recalls Birmingham Hip Resurfacing Acetabular Cups for Labeling Defects
Smith & Nephew is recalling six Birmingham Hip Resurfacing Acetabular Cups because they were distributed in the US with international labeling instead of FDA-approved instructions.
Product
Birmingham Hip Resurfacing Acetabular Cup with Impactor: (a) Size 56 mm, REF 74120156 (b) Size 64 mm, REF 74120164 (c) Size 54 mm, REF 74122154 (d) Size 58 mm, REF 74122158 (e) Size 60 mm, REF 74122160 (f) Size 62 mm, REF 74122162
Category
Medical Device
Distribution
7 states
LowFDA (Drugs)·D-0887-2018·2018-06-27
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurity Failures
Dr. Reddy's Laboratories is recalling specific lots of Atorvastatin Calcium tablets because they failed impurity and degradation specifications.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide