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. 1,955 recalls have been distributed to Ohio in the last 12 months.
Showing 21381–21400 of 30,087 recalls
Recalled Item: Lipase Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient...
The Issue: Medtronic Respiratory & Monitoring Solutions Announces a Voluntary Recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: Fetal patient report was automatically pulling prior measurement data for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uric Acid Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CinchLock SS Knotless Anchor with Inserter Recalled by Stryker Corporation...
The Issue: Stryker Endoscopy is recalling the CinchLock SS Knotless Anchor with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CinchLock Flex Knotless Anchor with Inserter Recalled by Stryker Corporation...
The Issue: Stryker Endoscopy is recalling the CinchLock SS Knotless Anchor with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distal Femoral Replacement (patient specific Recalled by Stanmore Implants...
The Issue: Incorrect component used to manufacture distal femoral replacement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Ceramic AHS Cluster-Hole Shell Recalled by Exactech, Inc. Due to...
The Issue: Devices were inadvertently sent to packaging and finished goods prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Tapered Recalled by Exactech, Inc. Due to Devices were...
The Issue: Devices were inadvertently sent to packaging and finished goods prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Tapered Recalled by Exactech, Inc. Due to Devices were...
The Issue: Devices were inadvertently sent to packaging and finished goods prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Tapered Recalled by Exactech, Inc. Due to Devices were...
The Issue: Devices were inadvertently sent to packaging and finished goods prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Splined Recalled by Exactech, Inc. Due to Devices were...
The Issue: Devices were inadvertently sent to packaging and finished goods prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Ceramic AHS Cluster-Hole Shell Recalled by Exactech, Inc. Due to...
The Issue: Devices were inadvertently sent to packaging and finished goods prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE Phototherapy system Recalled by Natus Medical Incorporated Due...
The Issue: The firm is adding the warning statement to the Instruction for Use for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PerFuse Decompression Instrument PN: 800-0541 Recalled by Biomet, Inc. Due...
The Issue: The Trocar and Plunger Assemblies are missing from the instrument, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVARREST Fibrin Sealant Patch Recalled by Ethicon, Inc. Due to Ethicon is...
The Issue: Ethicon is recalling EVARREST Fibrin Sealant Patch because the characters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0...
The Issue: Imaging system data may be displayed with an incorrect orientation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR Systems Unity PACS software Recalled by Merge Healthcare, Inc. Due to The...
The Issue: The software is not adding the correct tomo image.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.