FDA recall record

Imperative Care, ZOOM 71 Reperfusion Catheter, REF: ICRC071137, TRX Tip, 137 cm, 6F recall — FDA Z-2577-2021

There is a potential for distal end of catheters to fracture and become detached.

Class Iclassification
Z-2577-2021official record ID
Oct 6, 2021report date

Recall record at a glance

Official recordZ-2577-2021
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusCompleted
Recalling firmIMPERATIVE CARE Inc.
Report dateOct 6, 2021
Recall initiation dateAug 13, 2021
Quantity3118 units
LocationCampbell, CA, United States

Official product description

Imperative Care, ZOOM 71 Reperfusion Catheter, REF: ICRC071137, TRX Tip, 137 cm, 6F (.083 in/2.11 mm), .071 in/1.8 mm), STERILE.EO, Rx Only, UDI: (01) 00812212030191. For neurovascular procedures.

Why the product was recalled

There is a potential for distal end of catheters to fracture and become detached.

Distribution information

US nationwide distribution.

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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