LightPod ERA lasers recall
LightPod ERA lasers
Why was LightPod ERA lasers recalled?
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device
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?
LightPod ERA Lasers
- Product
- LightPod ERA lasers
- Recalling firm
- Aerolase Corporation
- Quantity
- 65
- Distribution
- US Nationwide Distribution
- Recall date
- January 15, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)