Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,099 recalls have been distributed to Kansas in the last 12 months.
Showing 4461–4480 of 50,117 recalls
Recalled Item: Ingenia Ambition X - For use as a diagnostic device Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S - For use as a diagnostic device Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Centurion Sterile CirClamp Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Product has been identified as having holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX - For use as a diagnostic device Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 -For use as a diagnostic device to obtain cross-sectional images...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T - For use as a diagnostic device Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S -For use as a diagnostic device to Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T- For use as Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 5300 - For use as a diagnostic device to obtain cross-sectional images...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X- For use as a diagnostic device to Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T - For use as a Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X - For use as a Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivier Sheer SPF 30 Mineral With Antioxidants (titanium dioxide 10% Recalled...
The Issue: Microbial Contamination of Non-Sterile Product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blue Tape Sriracha sauce is condiment Recalled by Blue Tape Sriracha Due to...
The Issue: Acidified product was manufactured by firm without ODA license.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mycophenolic Acid Delayed-Release Tablets USP Recalled by Ascend...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hammond's Dark Chocolate Filled Mini Waffle Cones Recalled by Hammond's...
The Issue: Undeclared allergen: milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mupirocin Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE Automatic Digital Blood Pressure Monitor Recalled by MEDLINE...
The Issue: It has been determined that certain Blood Pressure Monitors containing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 (Model Number 866060) Recalled by Philips...
The Issue: During a production process, Philips became aware of one IntelliVue power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.