Product Recalls in Ohio

Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,580 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,580 in last 12 months

Showing 2822128240 of 55,415 recalls

Medical DeviceApril 19, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Gentamicin Flex reagent cartridge Recalled by Siemens...

The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Maquet SAS

Recalled Item: VOLISTA StandOP (model 600) surgical lights shipped from October 2012...

The Issue: Potential keypad failure on VOLISTA StandOP Surgical Lights.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodApril 18, 2018· NatureBox, Inc.

Recalled Item: Whole Wheat Chocolate Animal Cookies Recalled by NatureBox, Inc. Due to...

The Issue: While packing from a bulk bin of whole wheat chocolate animal cookies, 2...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa...

The Issue: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder-Thai Maeng Da Recalled by Viable Solutions,...

The Issue: Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder-GREEN Horn Recalled by Viable Solutions, LLC...

The Issue: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Superior Foods Company

Recalled Item: Smoked Salmon Spread 5 lb. bulk units Recalled by Superior Foods Company Due...

The Issue: Superior Foods Company is voluntarily recalling a specific lot of Smoked...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 18, 2018· Canon Medical System, USA, INC.

Recalled Item: DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD) Recalled by Canon Medical...

The Issue: It was found when an operator performs a radiography using the wireless flat...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2018· Exsurco Medical

Recalled Item: Amalgatome SD Recalled by Exsurco Medical Due to Improper installation of...

The Issue: Improper installation of hand piece may result in a weakening of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2018· Tactical Medical Solutions, Inc.

Recalled Item: BLAST Bandage Recalled by Tactical Medical Solutions, Inc. Due to Blast...

The Issue: Blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2018· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...

The Issue: There is a potential for the cord to spark and cause a fire.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 17, 2018· Rhodes Pharmaceuticals, L.P.

Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only...

The Issue: Failed Dissolution Specification: Low dissolution outside of specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 16, 2018· Epic Products, LLC

Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...

The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 16, 2018· Cook Inc.

Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...

The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor Recalled by St Jude...

The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Promote Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing