FDAClass IIJanuary 24, 2024

Soltive SuperPulsed Laser System TFL Fiber Stripper recall: Sterility Concern

Soltive SuperPulsed Laser System TFL Fiber Stripper, Model Numbers TFL-AFS150, TFL-AFS200, TFL-AFS365, TFL-AFS550, TFL-AFS940

Why was Soltive SuperPulsed Laser System TFL Fiber Stripper recalled?

The strippers and cleavers are provided non-sterile and labelled as reusable/autoclavable. Olympus does not have validated cleaning and sterilization instructions. Use of a non-sterile fiber stripper or cleaver on a sterile fiber poses a risk of contamination.

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?

Lot Number: All units sold prior to 2023

Product
Soltive SuperPulsed Laser System TFL Fiber Stripper, Model Numbers TFL-AFS150, TFL-AFS200, TFL-AFS365, TFL-AFS550, TFL-AFS940
Recalling firm
Olympus Corporation of the Americas
Quantity
3001 units
Distribution
US Nationwide. Global Distribution
Recall date
January 24, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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