ReWalk Personal 6.0. Catalog number: 50-20-0004.
Reported: March 21, 2018 Initiated: August 14, 2017 #Z-0944-2018
Product Description
ReWalk Personal 6.0. Catalog number: 50-20-0004.
Reason for Recall
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
Details
- Recalling Firm
- Argo Medical Technologies Ltd
- Units Affected
- 127
- Distribution
- US and foreign.
- Location
- Haifahaifa
Frequently Asked Questions
What product was recalled? ▼
ReWalk Personal 6.0. Catalog number: 50-20-0004.. Recalled by Argo Medical Technologies Ltd. Units affected: 127.
Why was this product recalled? ▼
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 21, 2018. Severity: Moderate. Recall number: Z-0944-2018.
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