Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,798 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,798 in last 12 months

Showing 26612680 of 29,154 recalls

Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Medtronic Neurosurgery

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.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2024· Medtronic Neurosurgery

Recalled Item: Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER...

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.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health SMS Elastic Cuff Thumbhook Level 3 Isolation Gown Recalled...

The Issue: Isolation Gowns were manufactured with raw materials that may fail the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Cardinal Health 200, LLC

Recalled Item: Convertor Isolation Gown Recalled by Cardinal Health 200, LLC Due to...

The Issue: Isolation Gowns were manufactured with raw materials that may fail the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Securitas Healthcare LLC

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.

Class II — Potential Health HazardOngoing