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. 2,686 recalls have been distributed to Ohio in the last 12 months.
Showing 15561–15580 of 55,415 recalls
Recalled Item: ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...
The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...
The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...
The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Phenylbutyrate Powder Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Failed Impurities/Degradation Specifications; Out of Specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dairy Free Co. Dollup Lama Sour & Creamy Cashew Topping 4oz Recalled by...
The Issue: Quality Concerns on off taste
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The da Vinci Xi and X surgical systems (IS4000 and Recalled by Intuitive...
The Issue: Incorrect expiration date on its package labeling (shipper box and inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASC PneumoLiner device Recalled by Olympus Corporation of the Americas Due...
The Issue: Due to manufacturing error, the Pneumoliner Bag Distal Tab that exits the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Li-Ion Battery Pack Recalled by Datascope Corp. Due to A...
The Issue: A Cardiosave Lithium-Ion Battery Pack used during protocol testing failed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ CVxi Diagnostic Ultrasound Systems Recalled by Philips Ultrasound Inc...
The Issue: Ultrasound system software issue can cause an EchoNavigator error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mr. Nut brand Dried Oleaster Net Wt: 10.6 OZ (300g). Recalled by Vintage...
The Issue: Undeclared sulfites
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: The firm has confirmed the potential for ADVIA Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5MMX165MM CANNULATED SCREW Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The product label incorrectly indicated that the screws are fully threaded,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlipiZIDE Extended-Release Tablets Recalled by American Health Packaging Due...
The Issue: Failed Dissolution Specifications: results were above specification.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Injection Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Defective container: Cracked vials leading to lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIO-RAD BioPlex 2200 Syphilis Total & RPR Calibrator Recalled by Bio-Rad...
The Issue: Due to two issues: 1) Customer complaints associated with greater than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.