ReWalk Personal 6.0 recall
ReWalk Personal 6.0. Catalog number: 50-20-0004.
Why was ReWalk Personal 6.0 recalled?
Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Date range of Distribution: 09/01/2015 to 09/06/2017.
- Product
- ReWalk Personal 6.0. Catalog number: 50-20-0004.
- Recalling firm
- Argo Medical Technologies Ltd
- Quantity
- 127
- Distribution
- US and foreign.
- Recall date
- March 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)