Product Recalls in Kentucky
Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,111 recalls have been distributed to Kentucky in the last 12 months.
Showing 3901–3920 of 51,386 recalls
Recalled Item: ZoomMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VitalityXtra Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PeakMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZapMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica CI Analyzer. Catalog Numbers: 10947347. Recalled by Siemens...
The Issue: Potential that the IMT Diluent volume remaining (% remaining) does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Diagnostic Coil 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Breast Coil 3.0T 7ch Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Interventional Coil 3.0T Recalled by Philips North America Llc Due...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST SENSE Breast Dx Coil Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BYTE Aligner System BYTE All-Day Aligner System BYTE Recalled by Straight...
The Issue: Virtual-only clinical workflow utilized for dental aligners and impression...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 7ch 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 16ch 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 16ch 3.0T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Interventional Coil 1.5T Recalled by Philips North America Llc Due...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva TX Interventional Coil 3.0T Recalled by Philips North America Llc...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Diagnostic Coil 3.0T Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dS Breast 7ch 3.0T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Description: FACSLyric 2L6C Instrument US Recalled by Becton,...
The Issue: On October 18, 2024, BD has identified through customer complaints and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.