Palindrome RT Repair Kit 15 FR TAL 28cm, Sterile, Item Code 8888541128
FDA Recall Z-2366-2021 · Posted None
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Reason for Recall
This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
Firm Action
A Medical Device Market Withdrawal notification letter dated 5/28/21 was sent to customers.
Actions being taken by Medtronic
1. Medtronic is developing point-of-use labeling reinforcing the important user assembly steps contained within the IFU related to the hub/back end assembly procedure.
2. The IFU for Palindrome" RT and Palindrome" Precision RT chronic hemodialysis catheters will be updated to enhance the detailed instructions for users related to the steps required for hub/back end assembly.
Actions you should take
1. Please immediately quarantine and discontinue use of affected item codes and lots listed in Attachment A.
2. Please return affected product as indicated below. All unused products from the affected item codes and lots must be returned.
3. If you have distributed the Palindrome" RT and Palindrome" Precision RT chronic hemodialysis catheters listed in Attachment A, please promptly forward the information from this letter to those recipients.
4. Complete the Product Return Form even if you do not have inventory.
Purchased directly from Medtronic
1. Complete the Product Return Form and fax or email to Medtronic.
2. Ship affected product with RGA number provided by Customer Service to:
Medtronic
Attn: Field Returns
195 McDermott Road
North Haven, CT 06473 USA
Fax to 800-895-6140 or email to [email protected]
Credit for returned affected product will
be issued based on the RGA number.
Exception: Customers with zero inventory, fax to 651-367-2624 or email to [email protected]
Purchased from a distributor
1. Complete the Product Return Form and fax or email to Medtronic
2. Contact your distributor directly to arrange for return of product back to your distributor.
Fax to 651-367-2624 or email to [email protected]
This action is being taken with the knowledge of the FDA and other regulatory authorities. We request that you contact Medtronic if you experienced a quality problem or adverse event.
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Root Cause
Labeling design
Distribution Pattern
Worldwide distribution.
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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