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.
Showing 25101–25120 of 55,415 recalls
Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P) 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR 1.5T/3.0T Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia WT(P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dakota Specialty Milling Enhanced Flax Flour Blend Recalled by Dakota...
The Issue: An ingredient in the blended products has the potential to be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dakota Specialty Milling Milton's MG Premix w Enrichment 94503860 Recalled...
The Issue: An ingredient in the blended products has the potential to be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nutty Choco Pop Recalled by Funky Chunky LLC Due to Nutty Choco Pop has in...
The Issue: Nutty Choco Pop has in incorrect label and does not declare that it contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Phoenix AST-s Indicator Recalled by Becton Dickinson & Co. Due to Panels...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...
The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The WinStation Retinal Imager Recalled by Merge Healthcare, Inc. Due to...
The Issue: Certain configurations of Merge Eye Station hardware may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix AP AST Indicator Bag Recalled by Becton Dickinson & Co. Due to...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...
The Issue: When switching back & forth between multiple UV instances in the Windows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix AST Indicator Recalled by Becton Dickinson & Co. Due to Panels...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSOPT Ophthalmic Solution Recalled by Akorn Inc Due to Failed Stability...
The Issue: Failed Stability Specifications: out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.