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 7061–7080 of 55,415 recalls
Recalled Item: VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System Recalled by Ortho-Clinical Diagnostics, Inc....
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with:...
The Issue: Due to a trend in false positive Candida tropicalis results on blood culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm Recalled by In2Bones,...
The Issue: This Field Action is being conducted following the identification of a batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IdentiTi ALIF Standalone Interbody System: Part Number/Description...
The Issue: Due to reports of intraoperative graft bolt implantation breakages.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm Recalled by In2Bones,...
The Issue: This Field Action is being conducted following the identification of a batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SW Bari Lift & Transfer Recalled by Raye's Inc. Due to Retrospective...
The Issue: Retrospective engineering analysis against current ISO standards for hoists...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35 Recalled by...
The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Febuxostat Tablets Recalled by Amerisource Health Services LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic...
The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Opal Recalled by Synthes (USA) Products LLC Due to Products not sterilized,...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDSORB IPS Battery Pack Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX Recalled by Synthes...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: impression coping Recalled by Thommen Medical AG Due to The depth of the...
The Issue: The depth of the internal canal was not manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFNA Femoral Nail 11mm Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.