Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,145 recalls have been distributed to Indiana in the last 12 months.
Showing 3801–3820 of 53,528 recalls
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Otological Ventilation Tube - Donaldson - Blue Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - Donaldson - Double - Blue Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Double - Silicone Recalled by...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Silicone Recalled by Adept...
The Issue: Lack of 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Medical Biodesign Otologic Butterfly Graft Recalled by Cook Biotech,...
The Issue: Incorrect version of IFU was used rather than updated version; and incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Medical Biodesign Dural Graft Recalled by Cook Biotech, Inc. Due to...
The Issue: Incorrect version of IFU was used rather than updated version; and incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Medical Biodesign Hiatal Hernia Graft Recalled by Cook Biotech, Inc....
The Issue: Incorrect version of IFU was used rather than updated version; and incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.