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 29861–29880 of 55,415 recalls
Recalled Item: Iced Sugar Frosted Cookie Recalled by Midway Specialty Vehicles LLC Due to...
The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frosted Brownie Cookie Recalled by Midway Specialty Vehicles LLC Due to...
The Issue: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage:...
The Issue: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep...
The Issue: Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clofarabine injection Recalled by Sanofi-Aventis U.S. LLC Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert: authorized generic product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection Recalled by Genzyme...
The Issue: Labeling: Incorrect or Missing Package Insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kenny's Buckeye Pie Recalled by Kenny's Great Pies, Inc. Due to Undeclared Wheat
The Issue: Undeclared Wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...
The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag Recalled by...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCL 125 mg added to 0.9% Sodium Chloride 100 ml bag Recalled by...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate16 mg added to 0.9% Sodium Chloride 250 mL bag...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.