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. 1,932 recalls have been distributed to Ohio in the last 12 months.
Showing 24781–24800 of 30,087 recalls
Recalled Item: ROTROL P Control for ROTEM delta Thromboelastometry System Recalled by TEM...
The Issue: Some of vials were found to be partially filled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Imaging Tray (General Surgery convenience kit) Recalled by...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott m2000sp Recalled by Abbott Molecular Due to Some versions of...
The Issue: Some versions of Application Specifications (App Spec) are incompatible with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Pneumo Groups 2-14 Latex Test Recalled by Remel Inc Due to...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)...
The Issue: According to the recall notice received from Hospira, the recall was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within...
The Issue: A reagent within the test may return false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JResultNet drivers using ASTM coding language. Calculator/data processing...
The Issue: Software issue resulting in the results of one patient potentially being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) Recalled by...
The Issue: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Target 360 Standard 12mm x 30cm Recalled by Stryker Neurovascular Due to...
The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gateway OTW 2.75mm x 9mm Recalled by Stryker Neurovascular Due to Units of...
The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 20mm x 33cm Recalled by Stryker Neurovascular Due to Units of GDC...
The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 10mm x 30cm SR Recalled by Stryker Neurovascular Due to Units of...
The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 3mm x 6cm SR Recalled by Stryker Neurovascular Due to Units...
The Issue: Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HomeChoice/HomeChoice Pro Automated Personal Cycler Recalled by Baxter...
The Issue: The keypad buttons on HomeChoice devices may be activated without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Disposable Falope-Ring Band Applicator Kits. and Recalled by...
The Issue: All packages of Falope Ring Band Applicator kits are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS CardioImmune XL Cardiac Marker Control Recalled by Microgenics...
The Issue: MAS CardioImmune XL, level 1 (lot CXL16011), is showing vial-to-vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoracentesis & Paracentesis Procedure Tray Recalled by Pfm Medical Inc Due...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veta Peritoneal Catheter Kit Recalled by Pfm Medical Inc Due to PFM Medical...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6F x 60 cm Dual Lumen CT PICC Recalled by Pfm Medical Inc Due to PFM Medical...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASEPT 2000 ml Drainage Bag Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.