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. 1,146 recalls have been distributed to Ohio in the last 12 months.
Showing 6141–6160 of 30,087 recalls
Recalled Item: epoc BGEM Crea Test Card with epoc Host SW v3.37.3 Recalled by Siemens...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card (BUN & TCO2) Recalled by Siemens Healthcare Diagnostics...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM BUN Test Card with epoc Host SW v3.37.3 Recalled by Siemens...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium (Agar) (150mm) Recalled by Remel, Inc Due to...
The Issue: The test medium may not perform as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trexo Device Recalled by Trexo Robotics Holdings Inc. Due to Electrical...
The Issue: Electrical issues that could potentially render the device non-functional,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UFSK Treatment chair 500 XLE- Treatment chair for positioning and Recalled...
The Issue: Service life of the electrical seat part drive of the treatment chair may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Osteomed, LLC Due to Screws for osteotomies have contain an...
The Issue: Screws for osteotomies have contain an undersize screwhead which has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Specific...
The Issue: Specific diluent lot numbers showed that conductivity, osmolality, and pH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Shots were...
The Issue: Shots were terminated by the mAs integrator; however, the 4 ms exposure time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .14.500 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module Recalled by Abbott Laboratories Due...
The Issue: There are potential performance issues found in the Alinity ci-series System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) STANDARD OB PACK ASCENSION WI...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) PELVIC EXAM TRAY Recalled by...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) OPEN HEART TRACECART Recalled...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .14.800 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs...
The Issue: Weld protrusion/physical gap between the housing and pack cover, may exceed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.