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. 2,786 recalls have been distributed to Ohio in the last 12 months.
Showing 4621–4640 of 55,415 recalls
Recalled Item: LACRI-LUBE Recalled by AbbVie Inc. Due to Lack of Assurance of Sterility:...
The Issue: Lack of Assurance of Sterility: The impacted lots may contain a breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phasitron5 Breathing Circuit (P5-10 Recalled by Percussionaire Corporation...
The Issue: As a result of product complaints, breathing circuits are experiencing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu¿ VivaSight 2 DLT Endobronchial tube Recalled by Ambu Inc. Due to Ambu...
The Issue: Ambu has received complaints on Ambu¿ VivaSight 2 DLTs regarding hyper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Cystoscope Outer Sheath Recalled by Olympus Corporation of the...
The Issue: Product being removed due to incompatibility when used in conjunction with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S'mores Bites Recalled by Nuts.com Due to Undeclared Allergen
The Issue: Undeclared Allergen, milk - a mix-up between the product description and the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog...
The Issue: Olympus is removing the statement of compatibility with a GreenLight Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing...
The Issue: There is a potential for pinholes in the applicator pouch film which creates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Infusion System Recalled by Zyno Medical LLC Due to There is a defect...
The Issue: There is a defect in the air-in-line software algorithm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity m HPV AMP Kit Recalled by Abbott Molecular, Inc. Due to...
The Issue: Abbott has identified an increase of incidences regarding Error Code (EC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity m STI AMP Kit Recalled by Abbott Molecular, Inc. Due to...
The Issue: Abbott has identified an increase of incidences regarding Error Code (EC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Life2000 Ventilation System Recalled by Baxter Healthcare...
The Issue: The Life2000 ventilator may fail to initiate the Low Gas Pressure alarm if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Informatics Solution with software versions: 4.20 Recalled by...
The Issue: Synapsys software versions 4.20, 4.30, 5.10, 5.20, or 5.30 and utilizing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Aid Antiseptic Ointment Recalled by Zhejiang Jingwei Pharmaceutical...
The Issue: Incorrect/Undeclared Excipients: The inactive ingredients labeled on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: UroPass Ureteral Access Sheaths Product Name: Ureteral Access...
The Issue: Exposure of the UroPass product to Ultraviolet ( UV ) Radiation can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Infusion Pump. Product Number: 8637-20 Recalled by Medtronic...
The Issue: Potential for error and inability to interrogate pump due to data corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Universal Handle Recalled by Waldemar Link GmbH & Co. KG (Corp. Hq.)...
The Issue: Some lots of the LINK Universal Handle, with quick coupling, Stainless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minute Maid Zero Sugar Lemonade 12 cans carton Recalled by COCA COLA...
The Issue: Mislabeled. Cans of regular Minute Made Lemonade were placed in cartons...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1. Sqwincher Electrolyte Beverage Mix Recalled by Kent Precision Foods...
The Issue: Potential foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sqwincher Electrolyte Beverage Mix Recalled by Kent Precision Foods Group,...
The Issue: Potential foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: iCast Covered Stent Recalled by Atrium Medical Corporation Due to There is...
The Issue: There is an error in the Unique Device Identifier (UDI) printed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.