Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151
FDA Recall Z-0411-2020 · Posted None
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Recalling FirmAngiodynamics Inc. (Navilyst Medical Inc.)
Recall StatusTerminated
Product CodeGEI
Date Initiated2019-10-02
Date Terminated2020-07-29
Product Quantity30
Reason for Recall
The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay.
Firm Action
On October 2, 2019, AngioDynamics initiated a recall action by contacting customers by telephone and directing them to stop using the affected product and segregate until receipt of written the written recall notification. URgent Voluntary Medical Device Recall notification letters were sent to these customers on October 8, 2019.
1. Actions to be taken:
" IMMEDIATELY
o Stop using the product subject to recall.
o Remove any affected (recalled) product from your inventory (whether in labs, Central Supply,
Shipping and Receiving or ANY other location).
o Segregate this product in a secure location for return to AngioDynamics, Inc.
o Forward a copy of this recall notification to all sites to which you have distributed affected
product.
2. Complete and return the Reply Verification Tracking Form.
" If affected product is located in your institution, please call AngioDynamics Customer Service at 1-800-
772-6446 between 8:00 a.m. and 7:00 p.m. (Monday Friday: Eastern Standard Time) to obtain a
replacement or credit for your returned product.
" Promptly complete, sign, and return the enclosed Reply Verification Tracking Form (even if you do not
have any product to return); following the directions on this page and the Reply Verification Tracking
Form.
Email Reply Verification Tracking Form (preferred): [email protected]
Fax Reply Verification Tracking Form:
Attn: Talon Semi-Flex Recall Coordinator
Fax number 1-800-782-1357
3. Package and Return the Recalled Product.
" Package any product that is being returned in an appropriate shipping box.
" Write the RMA number on the RMA/Address label (provided on the Recall Verification Tracking Form)
and affix the label to the outside of the shipping box.
" To request a shipping label for returning product, please contact Customer Service (via recall email
address) for a prepaid FedEx label.
" Seal the box and return to:
AngioDynamics, Inc.
603 Queensbury Avenue
Queensbury, NY 12804
Attn: T
Root Cause
Under Investigation by firm
Distribution Pattern
The products were distributed to the following US states: LA, MA, OR, VA, and WA.
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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