FDA recall record

Clinical Innovations Kiwi Complete Vacuum Delivery System, Model No recall — FDA Z-2072-2020

There is a potential for loss of vacuum or failure to generate vacuum when using the firm's fetal vacuum delivery system.

Class IIclassification
Z-2072-2020official record ID
May 27, 2020report date

Recall record at a glance

Official recordZ-2072-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmClinical Innovations, LLC
Report dateMay 27, 2020
Recall initiation dateAug 6, 2019
Quantity2340 Units
LocationMurray, UT, United States

Official product description

Kiwi Complete Vacuum Delivery System, Model No. VAC-6000MTE - Product Usage: The Kiwi is a disposable vacuum-assisted fetal delivery system.

Why the product was recalled

There is a potential for loss of vacuum or failure to generate vacuum when using the firm's fetal vacuum delivery system.

Distribution information

OUS customers only.

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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