FDA recall record

Abbott Amplatzer Steerable Delivery Sheath (ASDS), REF ASDS-14F-075, is a percutaneous recall — FDA Z-2110-2023

There is an overall reported incidence rate of 0.77% related to observed or potential air embolism during procedures in which the ASDS product was used.

Class Iclassification
Z-2110-2023official record ID
Jul 19, 2023report date

Recall record at a glance

Official recordZ-2110-2023
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmAbbott
Report dateJul 19, 2023
Recall initiation dateJun 12, 2023
Quantity675 units
LocationPlymouth, MN, United States

Official product description

Abbott Amplatzer Steerable Delivery Sheath (ASDS), REF ASDS-14F-075, is a percutaneous catheter (cardiac).

Why the product was recalled

There is an overall reported incidence rate of 0.77% related to observed or potential air embolism during procedures in which the ASDS product was used.

Distribution information

Worldwide distribution - US Nationwide and the countries of Slovakia, Czech Republic.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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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