FDA recall record

UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile recall — FDA Z-0458-2022

The U-channel sheaths may cause damage to ProACT implant devices when the devices are passed through the sheath during a ProACT implantation procedure.

Class IIclassification
Z-0458-2022official record ID
Jan 12, 2022report date

Recall record at a glance

Official recordZ-0458-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmUromedica Inc.
Report dateJan 12, 2022
Recall initiation dateNov 22, 2021
Quantity18 devices
LocationPlymouth, MN, United States

Official product description

UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.

Why the product was recalled

The U-channel sheaths may cause damage to ProACT implant devices when the devices are passed through the sheath during a ProACT implantation procedure.

Distribution information

US Nationwide distribution in the states of AZ, CA, CO, KS, MD, TX, and WI.

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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