State

Tennessee product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

251–275 of 81577

SevereFDA (Drugs)·D-0026-2027·2026-10-14
Carolina Infusion Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable products due to a lack of assurance of sterility related to formulation and processing equipment.
Product
SEMAGLUTIDE/CYANOCOBALAMIN 9/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0030-2027·2026-10-14
FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 85/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
TIRZEPATIDE/CYANOCOBALAMIN 85/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936;
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0006-2027·2026-10-14
K.C. Pharmaceuticals Recalls Dry Eye Relief Eye Drops for Sterility Concerns
K.C. Pharmaceuticals is recalling 1,327,248 cartons of dry eye relief eye drops due to a lack of assurance of sterility. The products were distributed nationwide under multiple brand names.
Product
LEADER DRY EYE RELIEF EYE DROPS — LEADER DRY EYE RELIEF EYE DROPS (GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0071-2027·2026-10-14
Steris VERIFY Biological/Integrator Challenge Pack Recall for Spore Population Defect
Steris is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low, potentially causing false results in steam sterilization monitoring.
Product
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0036-2027·2026-10-14
Apothecary Pharma Recalls Tirzepatide Injection Vials Due to Sterility Concerns
Apothecary Pharma LLC is recalling 22 vials of Tirzepatide Injection due to a lack of assurance of sterility. The affected product was distributed nationwide.
Product
Tirzepatide Injection, 18mg/mL, 4 mL Sterile Multi-Dose Vial, Rx only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC 27513, NDC 85091-001-18.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0003-2027·2026-10-14
Good Sense Eye Drops Recalled for Lack of Sterility Assurance
K.C. Pharmaceuticals is recalling Good Sense Eye Drops Irritation Relief and related brands due to a lack of assurance of sterility.
Product
GOODSENSE EYE DROPS IRRITATION RELIEF — GOODSENSE EYE DROPS IRRITATION RELIEF (TETRAHYDROZOLINE HCL, ZINC SULFATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0008-2027·2026-10-14
K.C. Pharmaceuticals Recalls Multiple Brands of Eye Drops for Sterility Concerns
K.C. Pharmaceuticals is recalling multiple brands of eye drops, including Leader, Equate, and Walgreens, due to a lack of assurance of sterility.
Product
LEADER EYE DROPS REDNESS RELIEF — LEADER EYE DROPS REDNESS RELIEF (GLYCERIN, NAPHAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0086-2027·2026-10-14
Medline Bariatric Rollator Recalled Due to Front Wheel Detachment Risk
Medline is recalling 1,824 bariatric rollators because the front wheel assembly may detach, posing a risk of falls and serious injury.
Product
Rollator, Bariatric, Basic Steel, Burgundy, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWS
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26E071000·2026-10-14
KTM Recalls Steering Dampers for Super Duke Motorcycles
KTM is recalling certain Müller Präzision steering dampers for 2020-2026 KTM Super Duke R and Evo motorcycles because they can loosen, leading to loss of steering control.
Product
STEERING recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0088-2027·2026-10-14
Medtronic MiniMed Flex Insulin Pumps Recalled for Failed Verification Tests
Medtronic is recalling 20 MiniMed Flex insulin pumps that failed or lacked verification test results, posing risks of inaccurate insulin delivery and device malfunctions.
Product
Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product Description: The MiniMed Flex pump is an alternate controller enabled (ACE) pump intended for the subcutaneous delivery of insulin, at set and variable rates, for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0022-2027·2026-10-14
FDA Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0016-2027·2026-10-14
FDA Recalls X10 Supplement Containing Undeclared Sildenafil and Tadalafil
A&P CREATIONS is recalling X10 Natural Enhancement Supplement because it contains undeclared Sildenafil and Tadalafil.
Product
X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0002-2027·2026-10-14
K.C. Pharmaceuticals Recalls Artificial Tears Due to Sterility Concerns
K.C. Pharmaceuticals is recalling 505,896 cartons of artificial tears sold under multiple brands because the product lacks assurance of sterility.
Product
LEADER ARTIFICIAL TEARS 15 ML — LEADER ARTIFICIAL TEARS 15 ML (POLYVINYL ALCOHOL, POVIDONE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0020-2027·2026-10-14
Carolina Infusion Recalls Sermorelin Acetate Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Sermorelin Acetate 1 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
SERMORELIN ACETATE 1 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0028-2027·2026-10-14
Carolina Infusion Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling specific lots of Tirzepatide/Cyanocobalamin 64/2 mg/mL injectable because the product may lack assurance of sterility.
Product
TIRZEPATIDE/CYANOCOBALAMIN 64/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0018-2027·2026-10-14
Carolina Infusion Recalls Semaglutide Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Semaglutide 3 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
SEMAGLUTIDE 3 MG/ML INJECTABLE, 8 x 0.1 mL syringes, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0019-2027·2026-10-14
FDA Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
SEMAGLUTIDE/CYANOCOBALAMIN 3/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0017-2027·2026-10-14
FDA Recalls Tirzepatide Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tirzepatide 26 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
TIRZEPATIDE 26 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936;
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0074-2027·2026-10-14
Steris Recalls VERIFY Biological Steam Test Packs Due to Spore Population Concerns
Steris Corporation is recalling 217 VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false sterilization results.
Product
VERIFY Biological Steam Test Pack Model/Catalog Number: S3065
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0025-2027·2026-10-14
FDA Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used in compounding raised concerns about the product's sterility.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/60, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0007-2027·2026-10-14
K.C. Pharmaceuticals Recalls Good Sense Eye Drops for Sterility Concerns
K.C. Pharmaceuticals is recalling Good Sense Eye Drops Original Formula due to a lack of assurance of sterility. The recall affects 1,025,448 cartons distributed nationwide.
Product
GOODSENSE EYE DROPS ORIGINAL FORMULA — GOODSENSE EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0081-2027·2026-10-14
Safeguard US Operating LLC Recalls Compression Bandages Due to Degradation
Safeguard US Operating LLC is recalling 46,881 units of compression bandages and trauma kits because the bandages may be degraded, posing a risk of introducing foreign material into wounds.
Product
Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced, REF: 81-125-MC; Patrol IFAK II, Olive Drab, Stocked (Option 1), 81-129-OD; IFAK Bag, Intermediate, Black - Stocked, 81-133-BL; IFAK Bag, Intermediate…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0087-2027·2026-10-14
Medline Bariatric Rollator Recalled Due to Front Wheel Assembly Disconnect Risk
Medline is recalling 835 bariatric rollators because the front wheel assembly may disconnect from the frame, posing a risk of falls and severe injuries.
Product
Rollator, Bariatric, Basic Steel, Blue, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWBS
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·N/A·2026-10-14
White Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because testing found the active ingredient 7-hydroxymitragynine is present in a quantity greater than the labeled specification.
Product
SIERRA NEVADA CHEESE GRAZIERS RAW MILK SHARP CHEDDAR NET WT. 40 LBS Item 6516
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-0119-2027·2026-10-14
Intellijoint Navigation Systems Recalled for Potential Fire Risk
Intellijoint Surgical is recalling eight navigation systems because their workstations may contain a defective Apple battery that could overheat and cause a fire.
Product
Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249
Category
Medical Device
Distribution
Distributed nationwide