Ebi, Llc: 12 recalls on record

Recalls filed with 1 agency: FDA (12).

First recall on record: December 26, 2012. Most recent: May 1, 2024.

Risk classification: Class II: 12

Most recent recalls

DateAgencyProduct
May 1, 2024FDABiomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment o…Z-1617-2024
May 1, 2024FDA48" Lead Wires, Replacement Part Number: 1067724-4Z-1619-2024
May 1, 2024FDA20" Lead Wires, Replacement Part Number: 1067724-2Z-1618-2024
May 1, 2024FDABiomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatmen…Z-1616-2024
December 31, 2014FDASolitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b) 14-531594 Spring-…Z-0874-2015
June 25, 2014FDABiomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument for Spinal…Z-1811-2014
December 4, 2013FDAShortened Plug Driver; Low Volume Specialty Device; Qty:1; Rx Only; Non Sterile; Biomet S…Z-0411-2014
November 27, 2013FDABIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. …Z-0359-2014
October 9, 2013FDASolitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an intervertebral…Z-2292-2013
September 25, 2013FDACypher MIS Screw System, Biomet Spine Parsippany, NJ 07054. The Cypher MIS Screw System i…Z-2214-2013
March 27, 2013FDABiomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number 14-500178. The Po…Z-0954-2013
December 26, 2012FDABiomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178Z-0536-2013

Questions about this company

How many recalls does Ebi, Llc have?
Recalert has 12 U.S. recalls on record for Ebi, Llc, published between December 26, 2012 and May 1, 2024.
What was the most recent Ebi, Llc recall?
FDA recall Z-1617-2024, published May 1, 2024: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. Part Number:…
Which agencies have handled Ebi, Llc recalls?
Ebi, Llc appears as the recalling firm in recalls from: FDA (12).

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