FDAClass IIAugust 14, 2024

Soltive SuperPulsed Laser System Wireless Footswitch recall

Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL

Why was Soltive SuperPulsed Laser System Wireless Footswitch recalled?

Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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: TFL-AFSWL; UDI-DI: 00821925044258; Serial Numbers: All Serial Numbers.

Product
Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL
Recalling firm
Olympus Corporation of the Americas
Quantity
1,838 Units
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Canada, Chile, Germany, Hong Kong, Japan, Singapore.
Recall date
August 14, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls