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. 1,787 recalls have been distributed to Ohio in the last 12 months.
Showing 47941–47960 of 55,415 recalls
Recalled Item: Dollar General Triple Antibiotic Ointment Recalled by Faria Limited LLC dba...
The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senor Murphy Santa Fe Candymaker Peanut Brittle Recalled by Senor Murphy...
The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normative Data Template CD for use with the I-Portal devices. Used to...
The Issue: The data provided on the Normative Data Template CD for use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision RFD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA N Control Recalled by Horiba Instruments, Inc dba Horiba Medical...
The Issue: Horiba Medical is recalling the ABX PENTRA N Control because it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Propaq LT Series monitors. Model numbers 802LTAN Recalled by Welch Allyn...
The Issue: Welch Allyn will update Propaq 802 Series Vital Signs Monitor, models are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System....
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M ESPE Imprint II Regular Body Recalled by 3M Company - Health Care...
The Issue: Specific lots of Imprint II and Paradigm impression material packs are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Testing Disc Recalled by Remel Inc Due to...
The Issue: Individual discs in the lot may not be sufficiently impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Veris MR Monitor units The system is intended to Recalled by Medrad...
The Issue: The main board, P/N 301641, installed in some Medrad Veris MR Monitor units...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYSTEM 1E Liquid Chemical Sterilant Processing System Recalled by Steris...
The Issue: Customers indicated fluctuations in environmental conditions sites and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile...
The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hyperlyte CR (Multi-Electrolyte Concentrate) Recalled by B. Braun Medical...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefoxitin for Injection and Dextrose Injection Recalled by B. Braun Medical...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TrophAmine (10% Amino Acid Injection) Recalled by B. Braun Medical Inc Due...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 15% Amino Acids Injection PBP Glass Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.