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. 2,580 recalls have been distributed to Ohio in the last 12 months.
Showing 25941–25960 of 55,415 recalls
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...
The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...
The Issue: Cross contamination may have occurred between wells for the reagent pack. As...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...
The Issue: Software Update: External USB Drive performance and its impact on Graphic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altavera Levonorgestrel and Ethinyl Estradiol Tablets Recalled by Xiromed...
The Issue: Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SparkleFresh Fluoride Toothpaste Recalled by Medline Industries Inc Due to...
The Issue: Microbial Contamination of Non-Sterile Product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: treatNOW ABILIFY (aripiprazole) / ABILIFY MAINTENA 400-mg (aripiprazole) for...
The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: treatNOW ABILIFY (aripiprazole) and ABILIFY MAINTENA (aripiprazole) 400MG...
The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: robaxin-750 (methocarbamol tablets Recalled by Endo Pharmaceuticals, Inc....
The Issue: Labeling: Incorrect Instructions: Dosage information on the immediate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...
The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...
The Issue: Data loggers showed that one shipment to the United States experienced low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...
The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...
The Issue: The power supply unit for the printer used with the device can potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ E10 Ultrasound System Recalled by GE Healthcare, LLC Due to There...
The Issue: There is a potential for an undetected over temperature condition on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma...
The Issue: A detector can detach and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...
The Issue: The pouches of certain lots of product may have wrinkles along the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...
The Issue: The pouches of certain lots of product may have wrinkles along the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled by...
The Issue: The pouches of certain lots of product may have wrinkles along the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...
The Issue: Potential to lead to a false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.