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Terminated

Accurian RF Ablation, Cannula pk, Accurian, 100mm, 18G, 10mm, CS Product Number: AC0005 GTIN /UPN: 20763000153551 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting, and a stylet with a color-coded cap to indicate gauge size. The ACCURIAN RF Cannula included in the ACCURIAN RF Ablation Platform intended for the creation of radiofrequency lesions in nervous tissue.

FDA Recall Z-2690-2020 · Posted None

Recall StatusTerminated
Product CodeGEX
Date Initiated2020-06-08
Date Terminated2022-05-10
Product Quantity778 pk

Reason for Recall

Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.

Firm Action

Medtronic initiated both a voluntary correction notice pertaining to the labeling for the affected 20G and 22Gs and removal notice pertaining to the affected 18Gs on 10 June 2020. Notice of removal for ACCURIAN RF Cannula (18G, sterile, single-use) state the following action to be taken: 1) Locate and remove the impacted product from normal storage locations. Do not use this product. 2) Complete the enclosed Customer Confirmation Form and return via email to [email protected]. Please return this form to Medtronic even if you have no affected inventory. 3) As applicable, contact your Medtronic Sales Representative to coordinate the return and replacement of affected product. 4) Transmission of this Recall notification letter: a. This notification needs to be passed on to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. b. Please transfer this notice to other organizations on which this action has an impact. c. Please maintain a copy of this notice in your records. Safety Notification ACCURIAN RF Cannula (20G & 22G sterile, single-use) state the following action to be taken: Accurian RF cannula lot numbers identified may be used with adherence to the following mitigation: 1) In addition to following instructions within product IFU, the probe should be threaded straight into the center of the hub of the cannula. Do not insert a probe at an angle into the cannula. 2)If the probe catches in the cannula during insertion, remove and reinsert by threading straight into the center of the hub of the cannula.

Root Cause

Under Investigation by firm

Distribution Pattern

Worldwide distribution - US Nationwide distribution and the countries of Belgium and Australia.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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