Quick Facts at a Glance
- Recall Date
- December 18, 2025
- Hazard Level
- HIGH
- Brand
- Community Products
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Community Products
- Product type
- Gait Training Device
- Model numbers
- Model/Catalog Number: K660. ID Codes: K66020170425AA, K66020170612AA, K66020170621AA, K66020170622AA, K66020170626AA, K66020170626AB, K66020170626AC, K66020170627AC +12 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 18, 2025
Reported by FDA DEVICE
January 28, 2026
RecallRadar source check
February 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Potential for fraying on the body support strap.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Community Products, LLC or your healthcare provider for instructions. Notification method: E-Mail
About This Product
The E-Pacer is a gait training device designed to assist individuals in transitioning from sitting to standing. It is commonly used in rehabilitation settings for patients with mobility issues.
Why This Is Dangerous
The device's body support strap may fray, potentially causing it to fail during use. This could lead to falls or other injuries during rehabilitation exercises.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers may experience significant inconvenience as they must cease use of the E-Pacer and seek alternative mobility aids while waiting for further instructions.
Practical Guidance
How to identify if yours is affected
- Locate the model number on the device, which should be K660.
- Check the ID codes on the body support strap for any of the affected codes listed.
- Inspect the strap for signs of fraying or damage.
Where to find product info
The model number and ID codes are typically found on the device's label or near the power height adjustment mechanism.
What timeline to expect
Expect a response regarding refund or replacement within 4-6 weeks after contacting Community Products.
If the manufacturer is unresponsive
- Keep a record of all communications with the company.
- Contact your healthcare provider for additional guidance.
- Consider filing a complaint with the FDA if there is no response.
How to prevent similar issues
- Always check for recalls before purchasing medical devices.
- Look for devices with safety certifications and warranties.
- Inspect medical devices regularly for wear and tear.
Documentation advice
Keep copies of any emails, receipts, and correspondence related to the recall for your records.
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Product Details
The recalled E-Pacer is identified by Model/Catalog Number: K660. It was distributed worldwide, including the US, Canada, Australia, and several other countries. The affected units were sold under the Community Products brand.
Key Facts
- Fraying body support strap
- Stop using immediately
- Contact Community Products for instructions
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Safety Guide
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