Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,573 recalls have been distributed to North Dakota in the last 12 months.
Showing 2601–2620 of 27,512 recalls
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: 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: 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: 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: 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: 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: 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: 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: 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 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: 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: 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: 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: 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: FACSLyric 2L4C Instrument US Recalled by Becton, Dickinson and Company, BD...
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.
Recalled Item: FACSLyric 3L12C Instrument RUO Recalled by Becton, Dickinson and Company, BD...
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.
Recalled Item: FACSLyric 3L10C Instrument US-IVD Recalled by Becton, Dickinson and Company,...
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.
Recalled Item: FACSLyric 3L8C Instrument US-IVD Recalled by Becton, Dickinson and Company,...
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.
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.
Recalled Item: Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA...
The Issue: Due to complaints received reporting cracks and/or leaks of the stopcocks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.