Biomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument for Spinal Screw Fixation System.
This recall has been terminated (originally issued June 17, 2014).
- Company
- Ebi, Llc
- Recall Initiated
- May 15, 2014
- Posted
- June 17, 2014
- Terminated
- April 21, 2017
- Recall Number
- Z-1811-2014
- Quantity
- 32 units (30 domestic and 2 international)
- Firm Location
- Parsippany, NJ
- Official Source
- View on FDA website ↗
Reason for Recall
The Cypher MIS Screw Inserter may exhibit an increased rate of instrument tip failure.
Distribution
Worldwide Distribution - USA (nationwide) and the country The Netherlands.
Lot / Code Info
Catalog Number 14-501669; Lot Number 006731
Root Cause
Nonconforming Material/Component
Action Taken
Biomet sent an "Urgent Medical Device Recall Notice"/Fax Back Response Form dated May 15, 2014, via Fed Ex to all affected customers. The notice identified the product, the problem, and the action to be taken by the customer. Customers were instructed to inspect their inventory for the affected product and if located to remove the product from circulation; follow instructions on the attached Fax Back Response Form prior to return of the product; and return the product using the Fed Ex label included with the notification. Customers were instructed, if if they further distributed the product, they must notify their customers of the recall via the enclosed "Dear O.R. Manger" notice. If the customers had any questions they were asked to please contact Biomet, Monday through Friday (8 am to 5 pm) at 973.299.9300 xt. 2322.