State

Tennessee product recalls

20,324 recalls have nationwide distribution and so reach Tennessee. 0 additional recalls listed Tennessee specifically in their distribution scope.

About recalls in Tennessee

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Tennessee consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

13801–13825 of 20324

ModerateFDA (Drugs)·D-0474-2023·2023-03-29
Dofetilide Capsules Recalled for Failed Content Uniformity Specifications
Sun Pharmaceutical is recalling 1,920 bottles of Dofetilide Capsules (500 mcg) nationwide due to failed content uniformity specifications, meaning the capsules do not contain uniform amounts of active ingredient.
Product
Dofetilide Capsules, 500 mcg (0.5 mg), 60-count bottle, Rx only, Manufactured by: Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India, NDC 47335-0063-86
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1282-2023·2023-03-29
Contact Lens Recall: CooperVision Clariti 1-day Toric With Incorrect Power
CooperVision is recalling Clariti 1-day toric contact lenses from lot W0124677 because they were made with a misaligned axis that results in incorrect lens power.
Product
Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1283-2023·2023-03-29
DeRoyal Suction Canister Recalled Due to Lid Shrinkage Seal Defect
DeRoyal SafeLiner Suction Canister model PHESL-1000B is being recalled due to lid shrinkage that prevents proper vacuum seal formation and maintenance. The recall affects 27,200 devices distributed across multiple US states.
Product
DeRoyal SafeLiner Suction Canister, 1000cc, REF PHESL-1000B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0470-2023·2023-03-29
Daytrana Methylphenidate Patches Recalled for Defective Delivery System
Noven Pharmaceuticals is recalling specific lots of Daytrana methylphenidate transdermal patches distributed nationwide because the delivery system is out of specification for shear. The affected lots require patient and healthcare provider attention.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
HighCPSC·23739·2023-03-23
Arctic Cat Alterra 600 and Tracker 600 ATVs Recalled for Crash Hazard
Textron Specialized Vehicles is recalling about 3,800 Arctic Cat Alterra 600 and Tracker 600 all-terrain vehicles because the A-arm can separate from the frame, causing loss of steering control and crash risk.
Product
Arctic Cat Alterra 600 and Tracker 600 All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23163·2023-03-23
Kawasaki FT730V-EFI Lawn Mower Engines Recalled for Fuel Leak Fire Hazard
Kawasaki is recalling about 33,100 FT730V-EFI lawn mower engines due to a fuel line defect that can cause fuel leaks and fire hazards. Kawasaki has received four reports of incidents involving fuel line leaks, including one fire, with no injuries reported to date.
Product
Kawasaki FT730V-EFI Lawn Mower Engines
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23738·2023-03-23
Burnham Commercial Natural Gas Boilers Recalled for Burn Hazard
Burnham Commercial is recalling about 185 commercial natural gas boilers because delayed ignition and flame rollout can occur, posing a burn hazard. Two flame rollouts have been reported, but no injuries.
Product
Burnham Commercial Natural Gas Boilers
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1189-2023·2023-03-22
BALLARD ACCESS Closed Suction System Manifold May Crack and Leak
Avanos Medical is recalling 780 units of the BALLARD ACCESS Closed Suction System due to manifold cracking that can leak the respiratory circuit, potentially causing inadequate ventilation in neonatal and pediatric patients.
Product
BALLARD ACCESS Closed Suction System for Neonates/Pediatrics, Y-Manifold.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1190-2023·2023-03-22
Closed Suction System Manifold Cracking Poses Respiratory Circuit Leak Risk
Avanos Medical recalls BALLARD ACCESS Closed Suction System units due to manifold cracking, which can cause respiratory circuit leaks and inadequate ventilation in neonatal and pediatric patients.
Product
BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics, Elbow Manifold.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1238-2023·2023-03-22
BD Insulin Syringes Recalled Due to Nonsterile Condition
BD Insulin Syringes (Catalog 329420) are being recalled due to nonsterile conditions that could expose patients to pathogenic microorganisms and increase infection risk. The recall affects 961,000 units distributed worldwide.
Product
BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml, 12.7mm, 28G Single Unit Scale. Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329420
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0610-2023·2023-03-22
Soybean Lecithin Powder Recalled for Undeclared Peanut Allergen
Navada Imports is recalling 575 cases of soybean lecithin powder due to undeclared peanut allergen. Affected products were distributed nationwide to manufacturers.
Product
Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0463-2023·2023-03-22
Clobazam Tablets Recalled Due to Cross Contamination Risk
Breckenridge Pharmaceutical is recalling Clobazam 20 mg tablets (Lot #5210147, exp. 12/2023) nationwide due to potential cross contamination from manufacturing deviations.
Product
Clobazam Tablets, 20 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-901-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1246-2023·2023-03-22
Synthes TFN-Advanced Femoral Nail Recalled for Dimensional Labeling Mismatch
Synthes (USA) Products LLC is recalling TFN-Advanced Femoral Nails because labeled measurements do not match actual dimensions. Nails labeled 200mm may be 170mm and vice versa.
Product
TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.213S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0607-2023·2023-03-22
Sunflower Lecithin Powder Recalled for Undeclared Peanut Allergen
Navada Imports is recalling sunflower lecithin powder in 44 lb. boxes due to an undeclared peanut allergen. The affected product poses a serious risk to consumers with peanut allergies.
Product
Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1239-2023·2023-03-22
BD Insulin Syringes Recalled for Sterility Defect
Becton Dickinson recalls 1.9 million BD Insulin Syringes due to a nonsterility defect that could expose patients to pathogenic microorganisms and local infection risk.
Product
BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml, 12. 7mm, 28G Two Unit Scale- Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329424
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1240-2023·2023-03-22
BD Ultra-Fine Insulin Syringe 0.5mL Recalled for Nonsterility Risk
Becton Dickinson is recalling approximately 1.1 million BD Ultra-Fine Insulin Syringes due to nonsterility concerns. The affected syringes may expose patients to pathogenic microorganisms and risk of local infection.
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326713
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1248-2023·2023-03-22
TFN Femoral Nails dimensions mislabeled, may measure 170mm or 200mm
Synthes recalled TFN-Advanced Femoral Nails because some units have incorrect dimensions: nails labeled 200mm may measure 170mm, while those labeled 170mm may measure 200mm. This dimensional mismatch could compromise surgical fixation.
Product
TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Intended for temporary fixation and stabilization of proximal femur fractures Part Number: 04.037.242S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0581-2023·2023-03-22
Coffee pods with undeclared peanut residue being recalled
Two Rivers Coffee is recalling Brooklyn Bean Peanut Butter Cup Hot Cocoa pods because they may contain undeclared peanut residue. Consumers with peanut allergies should not use affected pods.
Product
Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single serve pods. Pods are packaged in the following Brooklyn Beans Variety Pack boxes: Brooklyn Beans Hot Chocolate Variety Pack Pods, 12 Count UPC:810683021977 Brooklyn Beans Brooklyn Beans Peanut Butter Chocolate Hot Coc
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0582-2023·2023-03-22
Pingo Hot Chocolate Pods Recalled for Undeclared Peanut Residue
Pingo hot chocolate pods may contain undeclared peanut residue. Consumers with peanut allergies should not consume affected products.
Product
Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 Count UPC: 810683028150 Pingo Hot Chocolate Pods Variety Pack, 100 Count UPC: 810683029805 Pingo Hot Ch
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1245-2023·2023-03-22
Fusion Bioline Vascular Graft recalled due to manufacturing straightness defect
Maquet Cardiovascular is recalling one Fusion Bioline Vascular Graft from lot 25162546 that failed straightness testing. The graft could reduce blood flow or cause tension, potentially leading to bleeding and pseudo-aneurysm.
Product
Fusion Bioline Vascular Graft, Part number M00201503046B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0459-2023·2023-03-22
Alprazolam Tablets Recalled Due to Potential Cross-Contamination Risk
Breckenridge Pharmaceutical is recalling multiple lots of Alprazolam 0.5mg tablets nationwide due to manufacturing process deviations that created a potential cross-contamination risk.
Product
Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: B
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0460-2023·2023-03-22
Alprazolam Tablets Recalled for Potential Cross-Contamination from Manufacturing Deviations
Breckenridge Pharmaceutical is recalling Alprazolam 1 mg tablets distributed nationwide due to manufacturing practice deviations that pose a potential cross-contamination risk.
Product
Alprazolam Tablets, USP, 1 mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0706-01), b) 500-count bottle (NDC 51991-0706-05) and c) 1,000-count bottle (NDC 51991-0706-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Bre
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0469-2023·2023-03-22
Eye allergy medication recalled for out-of-specification impurity
Teva Pharmaceuticals is recalling 715,632 bottles of Clear Eyes Once Daily eye drops due to an out-of-specification impurity found during stability testing.
Product
Clear Eyes, Once Daily, Eye Allergy Itch Relief, olopatadine hydrochloride ophthalmic solution, USP, 0.2%, Antihistamine, 2.5 mL (0.085 fl oz) bottle, Sterile, Distributed by Medtech Products Inc. Tarrytown, NY 10591, A Prestige Consumer Healthcare company, Made in Israel, UPC 67
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1244-2023·2023-03-22
BD Ultra-Fine II insulin syringes recalled for sterility defect
Becton Dickinson recalled 1,472,400 BD Ultra-Fine II insulin syringes due to a sterility defect. The nonsterile syringes pose a risk of local infection at injection sites.
Product
BD Ultra-Fine II Insulin Syringe 0.5mL, 8mm, 30G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326725
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1254-2023·2023-03-22
Amicus MNC Apheresis Kit at Risk of Stress Leak in Centrifuge Packs
Fenwal Inc is recalling certain batches of the Amicus MNC Apheresis Kit due to a potential for centrifuge packs to develop stress leaks. Affected units were distributed nationwide and internationally.
Product
Amicus MNC Apheresis Kit Double Needle. Component of Amicus Separator multiprocedural apheresis platform
Category
Medical Device
Distribution
Distributed nationwide