FDA recall record

Sedecal NOVA FA DR System. for diagnostic radiography recall — FDA Z-0488-2019

A safety problem with installation and maintenance could lead to the breakage of the two steel cables that support the equipment to its roof anchor. Due…

Class IIclassification
Z-0488-2019official record ID
Nov 28, 2018report date

Recall record at a glance

Official recordZ-0488-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSedecal S.A.
Report dateNov 28, 2018
Recall initiation dateJul 18, 2018
Quantity145 units
LocationAlgete, N/A, Spain

Official product description

Sedecal NOVA FA DR System. for diagnostic radiography.

Why the product was recalled

A safety problem with installation and maintenance could lead to the breakage of the two steel cables that support the equipment to its roof anchor. Due to this, the equipment may fall and cause harm to the patient, user, or third parties.

Distribution information

US and Canada

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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