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. 1,032 recalls have been distributed to Ohio in the last 12 months.
Showing 34561–34580 of 55,415 recalls
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (50 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes....
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...
The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100% APPLE CIDER 1 Gallon (3.78L) UV TESTED KEEP Recalled by Myers Cider...
The Issue: Myers Cider Mill LLC, of Monroeville, Ohio has issued a voluntary recall of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fruit 66 Tropical Punch Recalled by 1 Epic, LLC Due to 1 Epic is recalling...
The Issue: 1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fruit 66 Strawberry Melon Recalled by 1 Epic, LLC Due to 1 Epic is recalling...
The Issue: 1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fruit 66 Passion Fruit Mango Recalled by 1 Epic, LLC Due to 1 Epic is...
The Issue: 1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fruit 66 Mixed Berry Recalled by 1 Epic, LLC Due to 1 Epic is recalling...
The Issue: 1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sheridan/CF Recalled by Teleflex Medical Due to Labeling inconsistency -...
The Issue: Labeling inconsistency - units labeled with a 7mm tube may contain a size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Central Station Recalled by Spacelabs Healthcare Inc Due to The firm...
The Issue: The firm received reports of telemetry SpO2 numerics dropping off the Xhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCG (Chorionic Gonadotropin Lyopholized) II Recalled by Town and Country...
The Issue: Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zeasorb AF (miconazole nitrate) Recalled by GSK Consumer Healthcare Due to...
The Issue: Labeling Not Elsewhere Classified: front labels have the incorrect NDC or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...
The Issue: Sterility of the outer surface of the container compromised due to packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...
The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Gel Serum Protein Control: SPE Control Cat. No 5136 1 x 2.0 mL...
The Issue: Due to customer-experienced complaints on narrow assay range compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.