Recall Z-1781-2021

Clinical Laserthermia Systems AB · initiated April 1, 2021

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the Tranberg MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.

Codes / lots: Lot ID: 116540030718, 116540201117

Reason for recall

single use devices labeled as sterile may not have been adequately sterilized

FDA-determined cause: Equipment maintenance

Action taken

On April 1, 2021, CLS issued a "Field Safety Notice" concerning recalled product. In addition to informing consignees about the recall product, the firm asked consignees to take the following actions: 1. Please confirm upon receiving this letter that you hove taken port of the information in this field safety notice and forwarded a copy to relevant personnel within your organization by emailing the filled in reply form (appendix 1 ) to lotio.ljungberg@clinicolloser.com. 2. According to our documentation we hove shipped the concerned products to you. 3. We request you collect all concerned products remaining in your stock. We also request you to contact your customers/end users without delay to whom you hove distributed concerned products to, informing them about the product recall. You con use the information written in the first section of this letter. If the customer still has products in their stock, they should return these to you of their earliest convenience. 4. Furthermore, we request you to return all collected products from you and your customers' stock to CLS before 2021-04-30, Attention to Lotto Ljungberg, (the address is found below in this letter). All additional costs for this collection and return of products will be covered by CLS. 5. Please inform us how many products you will return by 4/15/21. Fill in the lower part of Appendix I when you hove identified the number of remaining products in you and your customer's stock.

Details

Recall number
Z-1781-2021
Initiated
April 1, 2021
Terminated
August 30, 2023
Product code
GEA – Cannula, Surgical, General & Plastic Surgery
Quantity
40 units
Distribution
Worldwide distribution - US Nationwide distribution in the states of TX, MD, CA and the countries of Canada, Germany, Switzerland.
Recalling firm
Clinical Laserthermia Systems AB, Lund

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1780-2021 Class IITranberg MR Cannula, REF: 4013-05, Rx Only, Sterile EO - Product Usage: used with the…single use devices labeled as sterile may not have been adequately sterilized 04/01/2021Terminated
Z-1782-2021 Class IITranberg Laser Applicator Non-cooled, 1.7mm/ 15G, 15 mm, Diffuser, 12 m, REF: 4017-02…single use devices labeled as sterile may not have been adequately sterilized 04/01/2021Terminated