Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
Summary
The FDA issued a Class II for Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180 by Boston Scientific Neuromodulation Corporation. Reason: Sterile anchors my lack sterility assurance..
Details
Source
Device Recall
External ID
Z-2404-2026
Action Date
2026-06-17
Status
Ongoing
Category
device
Product Description
Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
Lot/Code Info: GTIN: 08714729905318/Lot # 35107836
Quantity Affected: 43 units
Reason for Recall
Sterile anchors my lack sterility assurance.
Distribution
US Nationwide distribution in the states of MD, UT, FL, LA, SC, OK.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-29
Company
Valencia, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 228 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Boston Scientific Neuromodulation Corporation has 11 FDA actions in our database, including 10 recalls and 1 clearance.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Boston Scientific Neuromodulation Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Boston Scientific Neuromodulation Corporation have FDA actions?
Boston Scientific Neuromodulation Corporation has 11 FDA actions in our database, including 10 recalls and 1 device clearance.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2404-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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