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Stellex/CF Houston, LLC

Stellex/CF Houston, LLC Recalls

All product recalls associated with Stellex/CF Houston, LLC.

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Recall Summary

Total Recalls

1000

Past Year

353

Class I (Serious)

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 781–800 of 3680 recalls

Snack Tray (Wegmans) – Undeclared Allergens (2023)

Undeclared Gluten

Undeclared almonds and/or undeclared wheat

Class IIModerate

FDAJun 15, 2023IN, NY, PA• Stellex/CF Houston, LLC

Snack Tray (Wegmans) – Undeclared Allergens (2023)

Undeclared Gluten

Undeclared almonds and/or undeclared wheat

Class IIModerate

FDAJun 15, 2023IN, NY, PA• Stellex/CF Houston, LLC

Allura Xper X-ray System (Philips) – FlexMove Carriage Defect (2023)

The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

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Moderate

FDAJun 12, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Azurion 7 X-ray System (Philips) – FlexMove Carriage Defect (2023)

The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage.

Moderate

FDAJun 12, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Profile 0 AutoDrive Screw (Osteomed) – Screwhead Size Risk (2023)

Screws for osteotomies have contain an undersize screwhead which has the potential to pass through the plate hole.

Moderate

FDAMay 31, 2023Nationwide• Osteomed, LLC

MICRO-X Rover Mobile X-ray System (Micro-X) – Exposure Time Limitation (2023)

Shots were terminated by the mAs integrator; however, the 4 ms exposure time did not allow enough tolerance to achieve diagnostic exposures due to variations in hardware and how different timers are started.

Moderate

FDAMay 31, 2023Nationwide• Micro-X Ltd. Unit 14 6 Mab Eastern Promenade Tonsley Australia

Profile Zero Auto-Drive Screw (Osteomed) – Screwhead Size Risk (2023)

Screws for osteotomies have contain an undersize screwhead which has the potential to pass through the plate hole.

Moderate

FDAMay 31, 2023Nationwide• Osteomed, LLC

VEONEER BRAKE SYSTEMS BRAKE BOOSTER ASSEMBLY – veoneer brake systems, llc (veoneer) ... (2023)

Veoneer Brake Systems, LLC (Veoneer) is recalling certain Brake Booster assemblies with part numbers 4600A-TBA-A000, 4600A-TBA-A100, 4600A-TBF-A110, 4600A-TG7-A500, 4600A-TGS-A200, and 4600A-TYR-A100 installed in certain Honda vehicles. The tie rod fastener that connects the brake booster and the brake master cylinder may have been improperly assembled during manufacturing, which can cause the brake master cylinder to separate from the booster assembly.

High

NHTSAMay 24, 2023Nationwide• VEONEER BRAKE SYSTEMS

QUADROX-iD (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory s sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

Very High

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-iR (Maquet) – Packaging Accessory Damage (2023)

1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

Very High

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA

QUADROX-iD Pediatric (Maquet) – Packaging Pinhole Risk (2023)

Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.

Very High

FDAMay 18, 2023Nationwide• Maquet Medical Systems USA