FDA recall record

Covidien Beacon EUS Access System Preloaded Access 90degree Needle sterile, single-use recall — FDA Z-2768-2020

This voluntary recall is being conducted following three customer reports of the device cannula detaching during a procedure. In one case, the detached…

Class IIclassification
Z-2768-2020official record ID
Aug 12, 2020report date

Recall record at a glance

Official recordZ-2768-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCovidien LLC
Report dateAug 12, 2020
Recall initiation dateJun 26, 2020
Quantity375 units
LocationMansfield, MA, United States

Official product description

Beacon EUS Access System Preloaded Access 90degree Needle sterile, single-use, endoscopic ultrasound device consisting of a sharp stylet and an 18.5-gauge, echo-enhanced, tip-shaped, nitinol cannula intended to pierce tissue and then act as an access channel to facilitate guidewire placement to locations of the gastrointestinal tract.

Why the product was recalled

This voluntary recall is being conducted following three customer reports of the device cannula detaching during a procedure. In one case, the detached cannula was not retrieved during the procedure. Potential risks associated with a detached cannula include delay in treatment, biliary leak, pain and retained device fragments.

Distribution information

world wide distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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