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ALEXIS FIRE EQUIPMENT

ALEXIS FIRE EQUIPMENT Recalls

All product recalls associated with ALEXIS FIRE EQUIPMENT.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 2981–3000 of 25002 recalls

Alexis Fire Apparatus (Alexis Fire) – Electrical Wiring Problem (2024)

Fire/Burn Risk

Alexis Fire Equipment Company (Alexis Fire) is recalling certain 2022-2023 Apparatus fire trucks equipped with Weldon 8X16 Input-Output nodes. In the event of a short circuit or wiring failure, the firmware in the node may fail to shut off the output pin, resulting in overloaded electrical circuits.

High

NHTSAJan 9, 2024Nationwide• ALEXIS FIRE EQUIPMENT

OSOM BVBLUE Control Kit (Mckesson) – Temperature Excursion Risk (2024)

Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes .

Moderate

FDAJan 9, 2024Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Endo Cleaning Indicator (Mckesson) – Temperature Excursion Risk (2024)

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Moderate

FDAJan 9, 2024Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Outrageous Oat Cookies (Wegmans) – Undeclared Wheat (2024)

Undeclared Gluten

Product contains undeclared wheat.

Class IHigh

FDAJan 9, 2024DE, MD, MA +6 more• Wegmans Food Markets, Inc.

RotaFlow Centrifugal Pump (Maquet) – Sterile Barrier Risk (2024)

Nonconformities at their seal could potentially compromise the sterile barrier for affected products. Breach of sterile barrier could expose patients to pathogenic agents, resulting in the following potential harms: inflammation, infection, or sepsis.

High

FDAJan 8, 2024Nationwide• Maquet Medical Systems USA

RotaFlow Centrifugal Pump (Maquet) – Sterile Barrier Risk (2024)

High

FDAJan 8, 2024Nationwide• Maquet Medical Systems USA

Coachmen Galleria (Forest River) – Battery Wiring Problem (2024)

Forest River, Inc. (Forest River) is recalling certain 2020-2024 Coachmen Galleria motorhomes. The battery boost wiring may become damaged, resulting in an electrical short circuit and causing a loss of power steering.

High

NHTSAJan 8, 2024Nationwide• COACHMEN

Budesonide Tablets (Teva) – Failed Dissolution (2024)

Failed Dissolution Specifications

Class IIModerate

FDAJan 8, 2024Nationwide• Teva Pharmaceuticals USA, Inc

Benny T's Dry Hot Sauce (Vesta) – Unlisted Ingredients (2024)

The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.

Class IIModerate

FDAJan 8, 2024AL, AZ, CA +21 more• Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Benny T's Dry Hot Sauce Scorpion (Vesta) – Unlisted Ingredients (2024)

The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.

Class IIModerate

FDAJan 8, 2024AL, AZ, CA +21 more• Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Benny T's Dry Hot Sauce Very Hot (Vesta) – Unlisted Ingredients (2024)

The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.

Class IIModerate

FDAJan 8, 2024AL, AZ, CA +21 more• Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Hemostasis Probe (Olympus) – Mispackaging Concern (2024)

The BICOAG Hemostasis Probe with a coaxial plug was mispackaged into the package and labeled as a BICOAG Hemostasis Probe with a fixed pin connector.

Low

FDAJan 5, 2024Nationwide• Olympus Corporation of the Americas

OPTIMIZER CCM X11 Pulse Generator (Impulse Dynamics) – Therapy Delivery Risk (2024)

OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly detects a charging error. This may cause patients to experience heart failure symptoms similar to before implantation of the device.

High

FDAJan 5, 2024Nationwide• IMPULSE DYNAMICS (USA) INC

Rifampin Capsules 150mg (Lupin) – Subpotent Drug (2024)

Subpotent Drug and Failed Impurities/Degradation Specifications

Class IIModerate

FDAJan 5, 2024Nationwide• Lupin Pharmaceuticals Inc.

Rifampin Capsules 300mg (Lupin) – Subpotent Drug (2024)

Subpotent Drug and Failed Impurities/Degradation Specifications

Class IIModerate

FDAJan 5, 2024Nationwide• Lupin Pharmaceuticals Inc.

Fluocinolone Acetonide Oil (Glenmark) – Failed Specifications (2024)

Failed Excipient Specifications: OOS for assay of Isopropyl Alcohol

Class IIModerate

FDAJan 4, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

Zenzedi Tablets (Azurity) – Label Mix-up (2024)

Labeling: Label Mix-up

Class IHigh

FDAJan 4, 2024Nationwide• Azurity Pharmaceuticals, Inc.

Achieva 1.5T (Philips) – Quadrature Body Coil Safety Issue (2024)

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

High

FDAJan 3, 2024Nationwide• Philips North America

SmartPath to dStream (Philips) – Quadrature Body Coil Safety Issue (2024)

Laceration Risk

High

FDAJan 3, 2024Nationwide• Philips North America

Intera Achieva 1.5T Pulsar (Philips) – Quadrature Body Coil Safety Issue (2024)

Laceration Risk

High

FDAJan 3, 2024Nationwide• Philips North America