Important Medical Device Alerts

We have received recall notices for FreeStyle Libre 3 Sensors , TruAire-5 Oxygen Concentrators, and the Rifton TRAM & E-Pacer body support straps. Please review the official safety details now to ensure your equipment remains safe for continued use.

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Product Recalls & Safety Alerts

Product Safety & Recall Alerts

At Binson’s, your health, safety, and peace of mind are our highest priorities. We understand that learning about a product recall can be concerning, especially when you rely on that equipment for your daily well-being.

We are committed to transparency. This page serves as a central resource for current manufacturer recalls and safety notices affecting products we supply. Our goal is to provide you with clear information and actionable steps to ensure your continued safety.


Current Product Recalls

Please review the list below for recent safety alerts. If you use one of these devices, please click the link to view the official manufacturer documentation for specific instructions.

Date IssuedManufacturerProduct / DeviceSafety Notice TypeDocument
December 22, 2025RiftonK310, K320 TRAM & K660 E-Pacer
Body Support Straps
Voluntary Safety Notice Download Notice
November 24, 2025AbbottFreeStyle Libre 3 and FreeStyle Libre 3 Plus SensorsUrgent Medical Device Correction Download Notice
December 19, 2024Jiangsu Jumao X-Care Medical Equipment Co., Ltd.JMC5A Ni/TruAire-5 Oxygen Concentrator,
Model: O2C5L
Voluntary Recall Download Notice
Rifton TRAM & E-Pacer
Rifton

Affected: K310, K320, K660 Models (2012-2020)

Issued: December 22, 2025

Voluntary Safety Notice
Download Notice
FreeStyle Libre 3 Sensors
Abbott

Issued: November 24, 2025

Urgent Medical Device Correction
Download Notice
JMC5A Ni/TruAire-5 Oxygen Concentrator
Jiangsu Jumao X-Care Medical Equipment Co., Ltd.

Model: O2C5L

Issued: December 19, 2024

Voluntary Recall
Download Notice

 Important Note

If you do not see your specific device listed here but believe there may be an issue, please visit the FDA Medical Device Recalls Database for a comprehensive national list.

What to Do If Your Device Is Recalled

Finding out your equipment is part of a recall can be confusing. We recommend taking the following steps to manage the situation safely:

Stop and Verify

Do not panic. Read the safety notice carefully. Some alerts require you to stop using the device immediately, while others may simply require a software update or a specific part replacement.

Check Your Serial Number

Most recall notices will list specific "lot numbers" or "serial numbers" affected. Locate this number on your device (usually on the back or bottom) to confirm if your specific unit is included.

Follow Manufacturer Instructions

The linked documents above will provide the manufacturer's direct guidance. This often involves registering your device on their website to receive a repair kit or replacement.

Contact Us for Support

If you obtained your equipment through Binson's and need assistance interpreting the notice, our Customer Service team is here to help navigate the process.

Contact Customer Service
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