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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 2661–2680 of 29,228 recalls
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: Arial Server Software Versions 11.1.4 through 11.1.6 Recalled by Securitas...
The Issue: Certain software versions will not notify end users of calls initiated by...
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.