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 2568125700 of 55,415 recalls

Medical DeviceOctober 12, 2018· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...

The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· Stanley Security Solutions Inc

Recalled Item: M200 Fall Monitoring System Recalled by Stanley Security Solutions Inc Due...

The Issue: Damaged capacitor on the printed circuit board.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2018· St. Jude Medical, Inc.

Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....

The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...

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

Class II — Potential Health HazardOngoing
DrugOctober 11, 2018· Lannett Company, Inc.

Recalled Item: HydrOXYzine HYDROCHLORIDE SYRUP (HydrOXYzine Hydrochloride Oral Solution...

The Issue: CGMP Deviations: cleaning procedures during manufacturing caused out of...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 11, 2018· FOODSTIRS

Recalled Item: Foodstirs Modern Baking Recalled by FOODSTIRS Due to Individual pouches of...

The Issue: Individual pouches of Organic Minute Mug Cake Mix Celebration Confetti...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2018· Quest Nutrition, LLC

Recalled Item: Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - Recalled by Quest...

The Issue: Undeclared allergen; tree nut (almonds)

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 10, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...

The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...

The Issue: It was identified that the volume of air inside the mattress may expand in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Theragenics Corporation

Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...

The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2018· Synaptive Medical Inc

Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...

The Issue: This recall has been initiated due to a software defect found in the Guide...

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

Class I — Serious Health HazardOngoing
FoodOctober 9, 2018· World Variety Produce Inc.

Recalled Item: Melissa's Hatch Chile Clean Snax Recalled by World Variety Produce Inc. Due...

The Issue: Firm discovered that Hatch Chile Clean Snax lists peanuts in the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: ImmunoBooster Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: MenoPower Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Woman Power Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Body Skin Tonic Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund