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AGILITY FUEL SYSTEMS

AGILITY FUEL SYSTEMS Recalls

All product recalls associated with AGILITY FUEL SYSTEMS.

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Recall Summary

Total Recalls

1000

Past Year

353

Class I (Serious)

22

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 421–440 of 3680 recalls

Agility CNG Fuel System (Agility) – Fuel System Issue (2024)

Agility Fuel Solutions (Agility) is recalling certain Roof-Mounted, Tailgate-Mounted, and Front-of-Body Mounted CNG Fuel Systems. Please see the recall report for a complete list of part numbers. The manual cylinder valves may develop stress corrosion cracks in the bottom plugged port, causing a leak.

NHTSANov 20, 2024Nationwide• AGILITY FUEL SYSTEMS

Ricotta Stuffed Shells (Hungryroot) – Listeria Risk (2024)

Products have the potential to be contaminated with Listeria monocytogenes.

Class IIModerate

FDANov 20, 2024AZ, CA, DE +3 more• Joseph Epstein Food Enterprises, Inc. dba MamaMancini's

Stuffed Shells (Mama Mancini's) – Listeria Risk (2024)

1...20 212223 24...184

Page 22 of 184Next

Listeria

Products have the potential to be contaminated with Listeria monocytogenes.

Class IIModerate

FDANov 20, 2024AZ, CA, DE +3 more• Joseph Epstein Food Enterprises, Inc. dba MamaMancini's

Tec 820 ISO Vaporizer (GE Medical) – Anesthetic Delivery (2024)

Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.

FDANov 18, 2024Nationwide• GE Medical Systems, LLC

Tec 850 SEV Vaporizer (GE Medical) – Anesthetic Delivery (2024)

Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.

FDANov 18, 2024Nationwide• GE Medical Systems, LLC

Tec 820 SEV Vaporizer (GE Medical) – Anesthetic Delivery (2024)

Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.

FDANov 18, 2024Nationwide• GE Medical Systems, LLC

Tec 6 Plus Vaporizer (GE Medical) – Anesthetic Delivery (2024)

Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.

FDANov 18, 2024Nationwide• GE Medical Systems, LLC

Tec 850 ISO Vaporizer (GE Medical) – Anesthetic Delivery (2024)

Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.

FDANov 18, 2024Nationwide• GE Medical Systems, LLC

Bowl & Basket Onion Soup Mix – Undeclared Egg (2024)

Undeclared egg

FDANov 12, 2024IN, NJ• Gilster-Mary Lee Corporation Cake Plant

Philips Allura Xper Systems (Philips) – Lifetime Extension Issue (2024)

Potential safety issues in Allura Xper R7.6- R8.1 systems where the Lifetime Extension (LTE) kit is not installed in a timely manner. Root cause is under investigation, but the recall reason is listed as for systems over 10 years of life with LTE kits are experiencing propeller motor clamping bolt and x-ray tube locking bolt breaks. If this happens, it may cause erratic C-arm movements and potential collision with patients or bystanders, or detection of a false collisions and subsequent blocked movement of the c-arm. Movement may also cause image noise and black area on the x-ray image, and possible need to expose the patient to additional unnecessary radiation during re-examination.

FDANov 11, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Kreatech PapV-16 ISH Probe (Kreatech) – DNA fragment size issue (2024)

The DNA fragments for this specific lot number are too large, resulting in potential background around the cells due to suboptimal hybridization. An absence of signal could also be observed as a result of the suboptimal hybridization of the larger DNA fragments. The user may interpret potential background as a false positive result and an absence of signal as a false negative result, if proper positive and negative controls are not included.

FDANov 1, 2024FL, NY• Kreatech Biotechnology Bv Vlierweg 20 Amsterdam Netherlands

Tomographic Imager (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

Discovery MR750w 3.0T Scanner (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

SIGNA Architect AIR MRI (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

SIGNA Architect MRI System (GE Medical) – acoustic noise risk (2024)

Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.

FDAOct 28, 2024Nationwide• GE Medical Systems, LLC

MICRO-X Rover Mobile X-ray System (Micro-X) – Testing Defect (2024)

During internal testing it was found that if the system is Ready to expose and the hand switch is then dropped into the stowage unit such that it lands on the prep/expose switch, the prep switch can be activated for a very short time such that the orange ring of death is displayed in the tube cooling area of the screen. The system then becomes unresponsive to kV/mAs changes, prep/expose presses. The only way to proceed is to suspend the patient, Exit Nexus DR and relogin and continue the exam.

FDAOct 23, 2024Nationwide• Micro-X Ltd. Unit 14 6 Mab Eastern Promenade Tonsley Australia

MICRO-X Rover Mobile X-ray System (Micro-X) – Operation Requirements (2024)

Mobile x-ray system receiving/storage(operation) requirements to be followed: Temp:14 to 131(50 to 86) degrees F, RH:10% to 86%(30% to 60%) allow condensation dry time, Atmospheric Pressure:50kPa to 106 kPa(70kPa to 106kPa), Altitude:-102ft to 12,000 ft, (Maximum Gradient:9 degrees Fahrenheit), which mitigate risk of capacitor malfunction, unpredictable behavior, overheating, unintended start-up.

FDAOct 22, 2024CA, MD, TX +1 more• Micro-X Ltd. Unit 14 6 Mab Eastern Promenade Tonsley Australia

Vue PACS Viewer (Philips) – Calculation Errors (2024)

A software issue affecting Philips Vue PACS may cause incorrect ischemic map and table value calculations when using the export function in the Perfusion Application for a Siemens CT perfusion study, resulting in misdiagnosis due to incorrect ischemic map and table values.

FDAOct 10, 2024Nationwide• Philips Medical Systems Technologies Ltd. Matam Building 8/2 Advanced Technology Center Haifa Israel

Philips Zenition 70 (PHILIPS) – Mains Control Unit Fuse Issue (2024)

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

FDAOct 7, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Philips Zenition 50 (PHILIPS) – Mains Control Unit Fuse Issue (2024)

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

FDAOct 7, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands