State

Ohio product recalls

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

About recalls in Ohio

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 Ohio 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.

13826–13850 of 20324

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-1242-2023·2023-03-22
BD Insulin Syringes Recalled for Nonsterile Condition and Infection Risk
Becton Dickinson is recalling 686,500 units of BD insulin syringes due to a nonsterile condition that may expose patients to pathogenic microorganisms and risk of infection.
Product
BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Single Unit Scale-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329461
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-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-1262-2023·2023-03-22
da Vinci Surgical System Patient Cart Ballscrew Failure Risk
Intuitive Surgical recalls Patient Side Carts for da Vinci X and Xi surgical systems due to ballscrew failure risk. The failure could cause uncontrolled carriage movement leading to potential tissue injury during surgery. 9 units affected.
Product
Patient Side Cart, REF: 380620, with instrument arms, used as part of the da Vinci X Surgical System, REF: IS4200; Patient Side Cart, REF: 380652, with instrument arms, used as part of the da Vinci Xi Surgical System, REF: IS4000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1259-2023·2023-03-22
Radiation Therapy Software May Not Properly Execute Heart-Protection Breath Hold
Brainlab ExacTrac Dynamic software used in charged-particle radiation therapy systems may not properly execute Deep Inspiration Breath Hold (DIBH) functionality, a heart-protection technique. The issue affects 56 systems across the United States.
Product
Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1241-2023·2023-03-22
BD Insulin Syringes Recalled for Potential Nonsterile Condition
Becton Dickinson & Company is recalling 1.17 million BD Ultra-Fine Insulin Syringes due to a nonsterile manufacturing defect that could expose patients to pathogenic microorganisms and increase infection risk.
Product
BD Ultra-Fine Insulin Syringe 1mL, 6mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326678
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1256-2023·2023-03-22
Ambulance cot may separate due to insufficient epoxy in assemblies
Stryker's Power-PRO 2 ambulance cots may separate at head or foot due to insufficient epoxy. Four affected units in NY and VA should be removed from service immediately.
Product
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1249-2023·2023-03-22
Plato 17 Microcatheter Recalled Due to Loose Particle Risk
Scientia Vascular is recalling Plato 17 Microcatheters due to manufacturing defects that may introduce loose particles into the catheter lumen, potentially causing blood vessel blockage or inflammatory reactions.
Product
Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
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-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 (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 (Devices)·Z-1243-2023·2023-03-22
BD Ultra-Fine Insulin Syringes Recalled Due to Nonsterile Condition
Becton Dickinson is recalling BD Ultra-Fine Insulin Syringes (Catalog Number 326719) due to a nonsterile condition that could expose patients to pathogenic microorganisms and local infection. Approximately 80,500 units distributed worldwide are affected.
Product
BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1255-2023·2023-03-22
Medical Device Apheresis Kit Recalled Due to Stress Leak Risk
Fenwal Inc is recalling 6,564 units in certain lots of Amicus apheresis kits because centrifuge packs may develop a stress leak. No illnesses or injuries have been reported.
Product
Amicus Exchange Kit Therapeutics. Component of Amicus Separator multiprocedural apheresis platform
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1237-2023·2023-03-22
BD Ultra-Fine Insulin Syringe Recall Due to Nonsterile Manufacturing
Becton Dickinson is recalling 45,000 units of BD Ultra-Fine Insulin Syringes (catalog 326679, lot 2164338) due to nonsterile manufacturing that could expose patients to pathogenic microorganisms and local infection. Distribution was worldwide.
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326679
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 (Devices)·Z-1257-2023·2023-03-22
Beckman Coulter Access Immunoassay Analyzers Recalled for Defective Nut Bands
Beckman Coulter is recalling approximately 4,100 laboratory immunoassay analyzers due to defective nut bands that may cause operational failures and erroneous patient test results.
Product
Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N); (2) Access 2 Immunoassay Analyzer, Refurbished (386220); (3) Access 2 Immunoassay Analyzer, Refurbished (A65531) ; and (4) Access 2 Section, DxC 600i Packaged(A25640).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1258-2023·2023-03-22
Dimension Tacrolimus Diagnostic Cartridge Recalled for Measurement Imprecision
Siemens is recalling Dimension Tacrolimus diagnostic test cartridges (lots GA2286, GA3047, GA3171) due to confirmed measurement imprecision that could lead to incorrect drug dosing and potential organ failure or toxicity.
Product
Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test for the quantitative measurement of tacrolimus in human whole blood on the Dimension¿ clinical chemistry system SMN: 10700795 (DF207)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0609-2023·2023-03-22
Organic Sunflower Lecithin Powder Recalled for Undeclared Peanut Allergen
Navada Imports is recalling Organic Sunflower Lecithin Powder (44 lb boxes) due to undeclared peanut allergen. The product was distributed to a distributor in Missouri and then nationwide to manufacturers.
Product
Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0466-2023·2023-03-22
Buprenorphine Transdermal System 20 mcg/hour Recalled for Specification Failure
AVEVA Drug Delivery Systems recalls Buprenorphine Transdermal System 20 mcg/hour (Lot 51836) nationwide due to degradation product impurity exceeding specification limits during stability testing.
Product
Buprenorphine Transdermal System, CIII 20 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7079-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0580-2023·2023-03-22
Two Rivers Coffee pods recalled for undeclared peanut residue
Two Rivers Coffee hot cocoa pods in variety packs may contain undeclared peanut residue. Consumers with peanut allergies should not consume these products and should check the affected product codes.
Product
Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection packaged in single serve pods. Pods are packaged in the following Two Rivers Variety Pack boxes: -Two Rivers Coffee Hot Cocoa Pods, Single Serve Variety Sampler Pack , 40 Count UPC: 810683022554 -Two Rivers Coffee Hot C
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1251-2023·2023-03-22
BioFire BCID2 Diagnostic Panels Recalled for Temperature-Related Performance Issues
BioFire Diagnostics is recalling BioFire BCID2 diagnostic panels that experienced temperature excursions during shipment, which may reduce their performance. Affected kits were distributed in Florida and Georgia.
Product
In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - REF RFIT-ASY-0147
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1252-2023·2023-03-22
BioFire Respiratory Panel 2.1 Recalled Due to Temperature Shipping Excursions
BioFire Diagnostics is recalling BioFire Respiratory Panel 2.1 (RP2.1) diagnostic kits due to temperature excursions during shipping that may reduce device performance.
Product
In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1) - REF 423742
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1253-2023·2023-03-22
In Vitro Diagnostic GI Panel Recalled Due to Temperature Exposure During Shipping
BioFire Diagnostics is recalling FilmArray GI Panel diagnostic kits due to temperature excursions during shipping that may reduce test performance.
Product
In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - REF RFIT-ASY-0116
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0464-2023·2023-03-22
Evamist (Estradiol) Transdermal Spray Recalled for Failed Content Uniformity
Padagis US LLC is recalling 43,238 cartons of Evamist (Estradiol) transdermal spray nationwide because the spray content uniformity specification for standard deviation was not met at the 18-month stability time point.
Product
EVAMIST — EVAMIST (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide