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. 2,592 recalls have been distributed to Ohio in the last 12 months.
Showing 24821–24840 of 55,415 recalls
Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima PET/CT 560 Recalled by GE Healthcare, LLC Due to GE Healthcare PET/CT...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e700 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...
The Issue: There is a potential for the unit to catch fire due to one of the screen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e600 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...
The Issue: There is a potential for the unit to catch fire due to one of the screen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e500 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...
The Issue: There is a potential for the unit to catch fire due to one of the screen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...
The Issue: Packaged with an incorrect size inner cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...
The Issue: The optional Vacuum Unit may stop working and display the failure message...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...
The Issue: Incorrect needle length and gage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...
The Issue: Table tilts without operator involvement as a result of liquid spilling into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...
The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Watermelon Recalled by World Waters, LLC dba WTRMLN WTR Due to Cold Pressed...
The Issue: Cold Pressed Juice Watermelon WTRMLN WTR Original 12 packs due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Life-Line tm Catalytic Activated Energy Water Recalled by McDaniel Life-Line...
The Issue: Unapproved new drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.