EBI Patient Care, Inc. Recalls

Overview of recall records associated with EBI Patient Care, Inc., including dates, categories and classifications where available.

2recall records

May 31, 2017latest record date

May 31, 2017earliest record date

Recall history in this database

Classification mix: Class I: 2.

Medical DeviceMay 31, 2017

EBI Patient Care 10-1398M - SpF-PLUS Implantable Stimulator recall — FDA Z-2119-2017

Zimmer Biomet is conducting a medical device field action for the SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulator products due to higher than allowed cytotoxicity levels…

Class IFDA: TerminatedEBI Patient Care, Inc.

Medical DeviceMay 31, 2017

EBI Patient Care 10-1335M - SpF-XL IIB 2/DM Implantable Stimulator recall — FDA Z-2118-2017

Zimmer Biomet is conducting a medical device field action for the SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulator products due to higher than allowed cytotoxicity levels…

Class IFDA: TerminatedEBI Patient Care, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies EBI Patient Care, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.