Tranberg MR Cannula, REF: 4013-05, 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.
FDA Recall Z-1780-2021 · Posted None
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Recalling FirmCLINICAL LASERTHERMIA SYSTEMS AB
Recall StatusTerminated
Product CodeGAH
Date Initiated2021-04-01
Date Terminated2023-08-30
Product Quantity40 units
Reason for Recall
single use devices labeled as sterile may not have been adequately sterilized
Firm Action
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 [email protected].
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.
Root Cause
Equipment maintenance
Distribution Pattern
Worldwide distribution - US Nationwide distribution in the states of TX, MD, CA and the countries of Canada, Germany, Switzerland.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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