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AsttraZeneca Pharmaceuticals LP

AsttraZeneca Pharmaceuticals LP Recalls

All product recalls associated with AsttraZeneca Pharmaceuticals LP.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1341–1360 of 37661 recalls

Airsupra Inhalation Aerosol (AstraZeneca) – Delivery System Defect (2025)

Defective delivery system

Class IIModerate

FDAMay 14, 2025Nationwide• AsttraZeneca Pharmaceuticals LP

Ingenia 3.0T (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia Elition X (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDA

1...66 676869 70...1884

Page 68 of 1884Next

May 13, 2025

Nationwide

• Philips North America Llc

Ingenia 1.5T (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

MR 7700 (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia 1.5T CX (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia 1.5T S (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

MR 5300 (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Evolution Upgrade 1.5T (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Lago X (Spectral Instruments) – Label Mismatch (2025)

The X-ray safety and manufacturing date labels affixed to the Lago X/ AMI HTX instrument do not correspond exactly to the labeling stipulated by the FDA / CDRH.

Low

FDAMay 13, 2025Nationwide• Spectral Instruments Inc

Allon 2001 Device (Belmont Instrument) – Temperature Wrap Risk (2025)

An investigation into a report of the patient wrap (ThermoWrap), used with the Allon device, exceeding the set temperature determined that if: 1. The Human Sensor Board is disconnected from the Controller Board in the Allon device AND the temperature alarms are disabled, or 2. The Water In and Water Out and Thermostat sensors are disconnected from the Human Sensor Board AND the temperature alarms are disabled, the device will proceed to heat the water above the hardware fault limit without notifying the user of the faulty condition.

High

FDAMay 13, 2025Nationwide• Belmont Instrument LLC

SmartPath 1.5T (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

SmartPath Ingenia Elition X (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia 3.0T CX (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ingenia Ambition S (Philips) – Image Alignment Error (2025)

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Low

FDAMay 13, 2025Nationwide• Philips North America Llc

Ami HTX (Spectral Instruments) – Label Mismatch (2025)

The X-ray safety and manufacturing date labels affixed to the Lago X/ AMI HTX instrument do not correspond exactly to the labeling stipulated by the FDA / CDRH.

Low

FDAMay 13, 2025Nationwide• Spectral Instruments Inc