Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator , Stiffen Dilator, Nitinol Mandrel Wire w/ Radiopaque Tip [Au}, Needle, Extension Tube with Stopcock
FDA Recall Z-2917-2026 · Posted 2026-08-07
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Recalling FirmGalt Medical Corporation
Recall StatusOpen, Classified
Product CodeDQX
Date Initiated2026-06-26
Product Quantity114,260 kits
Reason for Recall
Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits.
Firm Action
On July 30, 2026, Galt Medical Issued a 4th iteration of the Urgent: Medical Device Recall Notification via Email expanding the affected lots. The initial notification was issued on June 26, 2026 via Email, 2nd notification issued on June 30, 2026 and 3rd notification issued on July 9, 2026. Galt Medical asked consignees to take the following actions
1. Discontinue use and distribution of the products with the affected lot numbers.
2. Examine your inventory, remove, and quarantine any identified devices with the affected lot numbers.
3. Ensure all applicable personnel within the vicinity of device activation carefully read the content of this notification. If affected product has been transferred to a different location, please ensure that location and personnel receive a copy of this notification
4. Complete the enclosed Field Correction Reply Forms and email or fax them to the attention of the Corrections Coordinator at [email protected] or 214-778-1433.
5. For additional details, see recall notification.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the state of MN.
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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