FDA recall record

Vascutek The Instructions for Use (IFU) for: Carotid Patch and Gelsoft Patch vascular recall — FDA Z-2543-2021

The devices contained the IFU for distribution to ROW (rest of world) consignees rather than U.S. consignees.

Class IIclassification
Z-2543-2021official record ID
Oct 6, 2021report date

Recall record at a glance

Official recordZ-2543-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmVascutek, Ltd.
Report dateOct 6, 2021
Recall initiation dateJul 8, 2021
Quantity159 total vascular grafts and patches
LocationInchinnan, N/A, United Kingdom

Official product description

The Instructions for Use (IFU) for: Carotid Patch and Gelsoft Patch vascular patches. FSN says Tapered Carotid Patch 920875t

Why the product was recalled

The devices contained the IFU for distribution to ROW (rest of world) consignees rather than U.S. consignees.

Distribution information

Distribution was made to PR and Guam.

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: E-Mail.

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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