Ohio recalls
3778 federal recalls on file affecting Ohio - 702 Ohio-specific plus 3076 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-01-14FDA-DeviceMeridian BioscienceClass IINationwideStop using Meridian Revogene C. difficile test
The affected lots show a decline in performance over time, which may lead to false-negative results.
- 2026-01-14FDA-DeviceRoche DiagnosticsClass IINationwideContact your lab if you used Roche Elecsys Anti-TSHR
Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or incorrect treatment.
- 2026-01-14FDA-DevicePhilipsClass IINationwideStop using affected Philips Incisive CT scanners
Potential for incomplete scan due to unstable connection inside of floating sensor.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideDo not use Halyard MINI PLUS KIT SOUTH
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideDo not use Halyard ORGAN RECOVERY OR PACK
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideStop using Halyard ORGAN RECOVERY OR PACK
Devices are not suitable for organ transplant.
- 2026-01-14FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS X-ray system
A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.
- 2026-01-14FDA-DeviceVision RTClass IINationwideCheck AlignRT InBore documentation for laser details
Vision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was omitted from the Instructions for Use for the subject system as required by 21 CFR 1040,10(h), via conformance with recognized consensus standard IEC 60825-1 Ed. 3 (FDA Laser Notice 56).
- 2026-01-14FDA-FoodMeijerClass IIStop using Meijer Steam Distilled Water
Floating black foreign substance in the product
- 2026-01-14FDA-FoodMAYEJClass IINationwideStop using MAYEJ Italian Parsley
pathogen Cyclospora cayetanensis
- 2026-01-14FDA-FoodZiyadClass IINationwideStop eating Baraka Gourmet Pastry Kunafe
May contain partially hydrogenated oils
- 2026-01-14FDA-FoodZiyadClass IINationwideCheck your Baraka puff pastry for recall
May contain partially hydrogenated oils
- 2026-01-14FDA-FoodAmbriolaClass IStop using Locatelli Grated Pecorino Romano
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Ambriola Piccante Pecorino Romano cheese
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano Grated cheese
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Sam's Pecorino Romano grated cheese
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano cheese
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Pinna Grated Pecorino Romano
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Locatelli Grated Pecorino Romano
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodAmbriolaClass IDo not eat Locatelli Grated Pecorino Romano
Product tested positive for Listeria Monocytogenes.
- 2026-01-14FDA-FoodSam Dry Fruits and NutsClass INationwideDon't eat Sam Dry Fruits & Nuts pistachios
Potential contamination with Salmonella.
- 2026-01-14FDA-DrugAvKAREClass IINationwideStop using AvKARE Rosuvastatin 10 mg tablets
Out of specification for dissolution.
- 2026-01-14FDA-DrugMedinaturaClass INationwideStop using ClearLife Allergy Nasal Spray
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
- 2026-01-14FDA-DrugMedinaturaClass INationwideStop using MediNatura ReBoost Nasal Spray
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
- 2026-01-14FDA-DrugSpecGxClass IINationwideCheck your SpecGx pain medication bottle
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
- 2026-01-14FDA-DrugSpecGxClass IINationwideCheck your SpecGx oxycodone tablets
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
- 2026-01-14FDA-DrugImprimisClass IINationwideStop using Imprimis Tri-Moxi eye injections
Presence of particulate matter - Glass like particles.
- 2026-01-14FDA-DrugImprimisClass IINationwideStop using Imprimis NJOF eye injection
Presence of particulate matter - Glass like particles.
- 2026-01-14FDA-DrugImprimisClass IINationwideStop using Imprimis eye injection immediately
Presence of particulate matter - Glass like particles.
- 2026-01-14FDA-DrugAlembic PharmaceuticalsClass IIINationwideStop using Alembic Fesoterodine Fumarate tablets
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
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