State

Ohio product recalls

73,584 recalls have nationwide distribution and so reach Ohio. 11,764 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total: 11,764
Critical: 2,117
Severe: 2,903
Most recent: 2026-10-21

Of the 11,764 recalls naming Ohio we have scored against our rubric, 2,117 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,903 (25%) are Severe.

Which agencies issued them

These figures cover only the 11,764 recalls whose distribution notice names Ohio specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

126–150 of 85348

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
SevereFDA (Devices)·Z-0075-2027·2026-10-14
Steris VERIFY Biological Steam Test Pack Recalled for Spore Population Defect
Steris Corporation is recalling VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false-negative steam sterilization results.
Product
VERIFY Biological Steam Test Pack Model/Catalog Number: S3069
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0032-2027·2026-10-14
FDA Recalls Tri-MIX Syringes Due to Sterility Assurance Concerns
Carolina Infusion, LLC is recalling Tri-MIX compounded syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/40, 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-0072-2027·2026-10-14
Steris VERIFY Biological Indicator Recall Due to Spore Population Concerns
Steris is recalling VERIFY Dual Species Self-Contained Biological Indicators because spore populations may fall below specifications, potentially leading to false sterilization results.
Product
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0004-2027·2026-10-14
K.C. Pharmaceuticals Recalls Leader Advanced Relief Eye Drops for Sterility Concerns
K.C. Pharmaceuticals is recalling Leader Advanced Relief Eye Drops and related brands due to a lack of assurance of sterility. The recall covers 208,896 cartons distributed nationwide.
Product
LEADER ADVANCED RELIEF EYE DROPS — LEADER ADVANCED RELIEF EYE DROPS (DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0037-2027·2026-10-14
Apothecary NAD+ Injection Recalled for Lack of Sterility Assurance
Apothecary Pharma is recalling NAD+ Injection vials due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vial, Rx Only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC, 27513, NDC 85091-011-06.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0108-2027·2026-10-14
Canon Medical Alphenix INFX-8000C/B5 Recalled for Tabletop Shift Risk
Canon Medical System is recalling one Alphenix INFX-8000C/B5 unit in Idaho due to a risk of tabletop shifting that could cause patient misalignment.
Product
Alphenix INFX-8000C/B5
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V673000·2026-10-14
Toyota Recalls Land Cruiser Hybrid Vehicles for Fuel Leak Risk
Toyota is recalling 2024-2027 Land Cruiser Hybrid vehicles because a fuel tube connection may disconnect and leak fuel, increasing fire risk.
Product
TOYOTA — TOYOTA LAND CRUISER HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0011-2027·2026-10-14
Better Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
The Better Bakehouse Snack Company is recalling Donutful Chocolate Dipped Vanilla Cake Donuts due to undeclared milk. The product was distributed nationwide.
Product
Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case. UPC 850041392103. Paperboard carton containing 5 individually wrapped packages of two donuts each. UPC: 850041392103. The Better Bakehouse Snack Co. 3651 Lindell…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-0020-2027·2026-10-14
Sweet Sensi THC Gum Drops Recalled for Staphylococcus aureus
Sweet Sensi is recalling Passion Guava Kush THC gum drops nationwide due to the detection of Staphylococcus aureus.
Product
Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable & flexible gold, purple and black metallic plastic mylar pouch and is sold in two sizes: 1) Net wt. Approx. 2.1oz (60g) 10 count and 2) Net wt. 6.3oz (180g) 30 count.…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0070-2027·2026-10-14
Steris VERIFY Biological/Integrator Challenge Pack Recall for Sterilization Monitoring Failure
Steris Corporation is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low to accurately monitor steam sterilization cycles.
Product
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0029-2027·2026-10-14
FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 76/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
TIRZEPATIDE/CYANOCOBALAMIN 76/2 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-0005-2027·2026-10-14
K.C. Pharmaceuticals Recalls Target Eye Drops for Sterility Concerns
K.C. Pharmaceuticals is recalling multiple brands of eye drops due to a lack of assurance of sterility. The recall covers 1,435,830 cartons distributed nationwide.
Product
TARGET EYE DROPS MAXIMUM REDNESS RELIEF EYE — TARGET EYE DROPS MAXIMUM REDNESS RELIEF EYE (GLYCERIN, NAPHAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0014-2027·2026-10-14
GIAS Food Inc. Recalls Lemon Alfredo Fettuccine for Listeria Contamination
GIAS Food Inc. is recalling 1,174 cases of Lemon Alfredo Fettuccine due to contamination with Listeria monocytogenes. The product was distributed to retail locations nationwide.
Product
Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 21 2027 L6081A, UPC 194346442706, DISTRIBUTED BY: Walmart Inc.…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0107-2027·2026-10-14
Polymedco Sediplast Tubes Recalled for Potential Blood Exposure
Polymedco is recalling Sediplast tubes because pressure buildup may eject the cap, releasing blood and creating a biological hazard for operators.
Product
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Category
Medical Device
Distribution
Distributed nationwide