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. 2,635 recalls have been distributed to Ohio in the last 12 months.
Showing 18401–18420 of 55,415 recalls
Recalled Item: TyTek PneumoDart- Intended for introduction into the body to facilitate...
The Issue: Updated IFU to inlclude: (1) identify the risks associated with the hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TyTek Tension Pneumothorax Access Kit TPAK10: 10 gauge Recalled by Tytek...
The Issue: Updated IFU to inlclude: (1) identify the risks associated with the hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EL-Anti-SARS-CoV-2 IgG Kit Recalled by Thera Test Laboratories, Inc. Due to...
The Issue: The cross-reactivity of the device may present an increased level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Recalled by Becton,...
The Issue: Recent product complaints showing an unexpected cell population exhibiting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic...
The Issue: Specific lots of MEDRAD Stellant FLEX 150 mL syringe kits may have holes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elastic Traction Device Recalled by Micro-Tech Usa Due to FDA has informed...
The Issue: FDA has informed Micro-Tech that the Elastic Traction Device is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Out-of-specification organic impurity results obtained during routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinnamon Apple Crisps packaged under the following Brands and sizes:...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Hatch Valley Salsa Recalled by Desert Premium Group, LLC Due to...
The Issue: One batch of salsa had a recorded equilibrium pH of 6.65.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with S. epidermidis E. coli and S. warneri.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Recalled by...
The Issue: Potential contamination with Escherichia coli Staphylococcus epidermidis and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO DISK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with Escherichia coli, Staphylococcus epidermidis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDI Novel Coronavirus COVID-19 IgG ELISA Kit Recalled by Epitope...
The Issue: The use of deionized water rather than distilled water during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...
The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COAPTITE Injectable Implant Recalled by Merz North America, Inc. Due to The...
The Issue: The Instructions for Use (IFU) updated 03/02/2020 does not match data listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XTANT Medical Recalled by XTANT Medical Due to Cervical Implants contain a...
The Issue: Cervical Implants contain a label that incorrectly identifies the grade of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.