ReWalk Personal 6.0. Catalog number: 50-20-0004.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Date range of Distribution: 09/01/2015 to 09/06/2017.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Argo Medical Technologies Ltd
- Reason for Recall:
- Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
ReWalk Personal 6.0. Catalog number: 50-20-0004.
Product Codes/Lot Numbers:
Date range of Distribution: 09/01/2015 to 09/06/2017.
Distribution:
Distributed in: US
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0944-2018
Related Recalls
Class I - Dangerous
ReWalk Robotics received two complaints (one in the US; one in the Germany), which alleged that the ReWalk device waistpack (which is the location of the Li-Ion battery packs) caught fire while being charged.