FDA Recall Open, Classified

Soltive SuperPulsed Laser System TFL FIBER CLEAVER, Model Number TFL-AFC

Recall: Z-0717-2024 · Initiated December 4, 2023

Recall

Recall Number
Z-0717-2024
Event Number
93613
Firm
Olympus Corporation of the Americas
FEI Number
2429304
Product Code
GEX
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
December 4, 2023
Posted
January 12, 2024
Address
3500 Corporate Pkwy, Center Valley, PA, 18034-8229

Description

Soltive SuperPulsed Laser System TFL FIBER CLEAVER, Model Number TFL-AFC

Reason

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.

Action

An URGENT: MEDICAL DEVICE REMOVAL notification letter dated 12/4/23 was sent to customers. Actions to be taken by the end user: Our records indicate that your facility has received one or more affected units. Olympus requests you to take the following actions: 1. Examine your inventory and quarantine any devices with the lot number specified above. 2. Please contact Olympus customer service representative at 1-800-848-9024, option 2, with the quantity and model of affected devices. Olympus will issue a Return Material Authorization to return any affected product at no charge. Olympus will issue a credit to your facility upon return of affected product. 3. Access the Olympus recall portal to indicate that you have received this notification. a. Go to https://olympusamerica.com/recall. b. Enter the recall number "0435 c. Complete the form as instructed. 4. If you have distributed these devices outside your facility, please provide a copy of this letter to those facilities immediately. Olympus requests you to report any complaints, including product labeling issues, to our Technical Assistance Center (TAC) at 1- 800-848-9024, option 1, and the FDA. Adverse events experienced with the use of this product may also be reported to the FDA s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax. Olympus fully appreciates your prompt cooperation in addressing this situation. If you require additional information, please do not hesitate to contact me directly by phone at (647) 999-3203 or by e-mail at [email protected].

Distribution

US Nationwide. Global Distribution

Quantity

236 units