State

Tennessee product recalls

73,741 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,859
Critical: 1,324
Severe: 1,973
Most recent: 2026-10-28

Of the 7,859 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 1,973 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32951–32975 of 81600

SevereFDA (Devices)·Z-1333-2020·2020-02-26
Siemens Uroskop Omnia max Recalled for Collision Control Override Risk
Siemens is recalling 192 Uroskop Omnia max devices because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.
Product
Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1272-2020·2020-02-26
Philips HeartStart AEDs Recalled for Quality Standards Defect
Philips is recalling 96 HeartStart AEDs because their Printed Circuit Assemblies were not manufactured or repaired to quality standards.
Product
Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED, Model 861304, HSI codeRev: E.03.063
Category
Medical Device
Distribution
9 states
SevereFDA (Devices)·Z-1286-2020·2020-02-26
Recall of Polysorb Sutures Due to Potential Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could impact sterility.
Product
Polysorb Braided Absorbable Suture 2-0 VIOLET 30" V-20, Item Code GL123 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0708-2020·2020-02-26
Dragonfly Botanicals Breathe Deep Recalled for Internal Use of Coltsfoot
Green Water, LLC is recalling Dragonfly Botanicals Breathe Deep dietary supplements because they contain Coltsfoot, which is not to be used internally.
Product
Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement, sold in 0.5 oz, 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0707-2020·2020-02-26
Taspen's Organics Breathe Easy Herbal Tincture Recalled for Coltsfoot
Green Water, LLC is recalling Taspen's Organics Breathe Easy Herbal Tincture because it contains Coltsfoot, which is not to be used internally.
Product
Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement, sold in 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1290-2020·2020-02-26
Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20, Item Code GLS322 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0724-2020·2020-02-26
Safeway Chocolate Buttercreme Base Recalled for Plastic Polymer Contamination
CSM Bakery Products is recalling 45 lb. boxes of Safeway Chocolate Buttercreme Base because pieces of plastic polymer were introduced into the sugar system.
Product
45 lb. box SAFEWAY CHOCOLATE BUTTERCREME BASE, MDM # 10201865, Distributed by Safeway Inc. PO Box 99 Pleasanton, CA 94566-0009
Category
Food
Distribution
Distributed nationwide
HighCPSC·20078·2020-02-26
Safavieh Recalls Aura and Silas Chests Due to Tip-Over Hazards
Safavieh is recalling Aura and Silas 3-drawer chests because they can tip over or entrap children if not anchored to the wall.
Product
Aura and Silas 3-Drawer Chests
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1264-2020·2020-02-26
Recall of Covidien Endo GIA Ultra Universal Staplers Due to Sterility Risk
COVIDIEN LLC is recalling 2,180 units of Endo GIA Ultra Universal Staplers because the sterile barrier may be compromised, increasing the risk of infection.
Product
Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection, transection in general surgery Item Code: EGIAUSTND
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1314-2020·2020-02-26
Nobel Biocare Dense Bone Drill Recall Due to Sterility Concerns
Nobel Biocare is recalling Dense Bone Drills because a packaging sealing issue may compromise sterility during shelf life.
Product
Dense Bone Drill NP 3.5x16 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0723-2020·2020-02-26
CSM Bakery Products Recalls Donut Icing Due to Plastic Polymer Contamination
CSM Bakery Products is recalling 43 lb. pails of Glossy White Icing distributed by Krispy Kreme because pieces of plastic polymer were introduced into the sugar system.
Product
43 lb. pail GLOSSY WHITE ICING (1102507) donut icing, MDM # 10199098, Distributed by Krispy Kreme Doughnut Corporation 1814 Ivy Avenue, Winston-Salem, NC 27105
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1235-2020·2020-02-26
Cardinal Health Recalls Presource Procedure Packs with Potential Sterility Issues
Cardinal Health is recalling Presource Procedure Packs containing AAMI Level 3 surgical gowns because they may not be sterile due to improper environmental conditions during manufacturing.
Product
Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020. Additional kits produced through February 19, 2020 were included.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1315-2020·2020-02-26
Nobel Biocare Dense Bone Drills Recalled for Sterility Concerns
Nobel Biocare is recalling Dense Bone Drills because a packaging defect may compromise sterility during shelf life.
Product
Dense Bone Drill WP 5x13 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V111000·2020-02-26
Custom Fire Recalls 2017 Side Mount Pumper for Foam Pump Overheating
Custom Fire is recalling one 2017 Side Mount Pumper because the foam pump system can overheat and fail, making firefighting foam unavailable.
Product
CUSTOM FIRE — CUSTOM FIRE SIDE MOUNT PUMPER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1332-2020·2020-02-26
Siemens Luminos Agile Max X-ray System Recalled for Collision Risk
Siemens is recalling 475 Luminos Agile Max X-ray systems because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.
Product
Luminos Agile Max, Model No. 10762472 - Product Usage: Luminos Agile Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1319-2020·2020-02-26
Nobel Biocare Recalls Implant Retrieval Instruments Due to Sterility Concerns
Nobel Biocare is recalling 423 implant retrieval instruments because a packaging defect may compromise sterility during shelf life.
Product
Implant Retrieval Instrument CC NP & Ext Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1329-2020·2020-02-26
Philips CombiDiagnost PCF X-ray System Software Recall
Philips is recalling 131 CombiDiagnost PCF X-ray systems due to a software error that locks the table and an incorrectly installed thermos switch.
Product
CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1282-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Packaging Integrity Issues
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may compromise sterility.
Product
Polysorb Braided Absorbable Suture 1 36 VIOLET GS-24, Item Code CL915 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1337-2020·2020-02-26
Siemens Luminos dRF Max Recalled for Software Bug Affecting Patient Images
Siemens Medical Solutions USA, Inc. is recalling 46 Luminos dRF Max digital radiography systems due to a software bug that may assign one image to two different patients, potentially affecting medical diagnosis.
Product
Luminos dRF Max, model no. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1311-2020·2020-02-26
Nobel Biocare Dental Drills Recalled Due to Packaging Seal Defects
Nobel Biocare is recalling 264 tapered dental drills because a packaging sealing defect may compromise sterility during shelf life.
Product
Drill Tapered WP 5x10 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0725-2020·2020-02-26
CSM Bakery Products Recalls Simplicious Cream Cheese Icing Due to Plastic Contamination
CSM Bakery Products is recalling 18 lb. pails of Simplicious Cream Cheese Icing because pieces of plastic polymer were introduced into the sugar system.
Product
18 lb. pail SIMPLICIOUS CREAM CHEESE ICING 18#PL, MDM # 10202840, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
HighNHTSA·20V113000·2020-02-26
Thomas Built Buses Saf-T-Liner C2 Recall for Exterior Light Failure
Daimler Trucks North America is recalling 2017-2020 Thomas Built Buses Saf-T-Liner C2 school buses because the exterior warning lights and stop sign may fail, increasing injury risk.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0729-2020·2020-02-26
CSM Bakery Products Recalls Donut Icing Due to Plastic Polymer Contamination
CSM Bakery Products is recalling 43 lb. pails of White 'n Glossy Icing donut icing because pieces of plastic polymer were introduced into the sugar system.
Product
43 lb. pail WHITE 'N GLOSSY ICING donut icing, MDM # 10203280, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1233-2020·2020-02-26
Siemens Dimension Vista Enzymatic Creatinine Reagent Recalled for Interference
Siemens Healthcare Diagnostics is recalling Dimension Vista Enzymatic Creatinine reagent because it may produce falsely depressed results for patients taking phenindione.
Product
Dimension Vista Enzymatic Creatinine (ECREA) reagent, SMN 10700444
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1317-2020·2020-02-26
Nobel Biocare Implant Retrieval Instruments Recalled for Sterility Concerns
Nobel Biocare is recalling 197 implant retrieval instruments because a packaging defect may compromise sterility during shelf life.
Product
Implant Retrieval Instrument Hex & Tri-Chi NP/RP 31mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
Category
Medical Device
Distribution
Distributed nationwide