FDA recall record

EBI 48" Lead Wires, Replacement Part Number: 1067724-4 recall — FDA Z-1619-2024

Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being…

Class IIclassification
Z-1619-2024official record ID
May 1, 2024report date

Recall record at a glance

Official recordZ-1619-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmEBI, LLC
Report dateMay 1, 2024
Recall initiation dateMar 22, 2024
Quantity594 units (2 lead wires assembly)
LocationParsippany, NJ, United States

Official product description

48" Lead Wires, Replacement Part Number: 1067724-4

Why the product was recalled

Damage to the lead wire sheath (black cable) component and causing exposure of the wires, potentially lead to no therapeutic treatment signal being delivered to the electrodes, and result in delay of treatment

Distribution information

US Nationwide distribution.

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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