Drop Arm Versamode" recall
Drop Arm Versamode"
Why was Drop Arm Versamode" recalled?
The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
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?
Model: 6810A; Device Identifier: M36868101; and Lot number: BMW316BS
- Product
- Drop Arm Versamode"
- Recalling firm
- Gf Health Products
- Quantity
- 66 units
- Distribution
- Distributed nationwide to CA, WI, PA, IL, and TX. Distributed internationally to Mexico and Canada.
- Recall date
- April 14, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)