Z-1406-2021 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- April 21, 2021
- Initiation Date
- March 5, 2021
- Termination Date
- August 2, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 49 devices
Product Description
Prodisc C - prosthesis, intervertebral disc - Product Usage: indicated in skeletally mature patients for reconstruction of the disc from C3-C7 following single-level discectomy for intractable symptomatic cervical disc disease (SCDD), Part number: 09.820.055S
Reason for Recall
Centinel Spine learned through five customer complaints that the product was missing the "UP" etching on the superior plate of the prodisc C device. Per the Surgical Technique, the "UP" is one of the methods used to indicate the direction in which the surgeon should place the prodisc C into intradiscal space. There are also "UP" indications in the packaging and on instrumentation as additional guides to help the surgeon properly implant the device that were present for the affected product.
Distribution Pattern
US Nationwide distribution in the states of CA, MD, DC, TN, GA, NC, PA, KY, NY, AZ, CO, OH, FL, MI.
Code Information
UDI (01)00843193112842(17)241231(10)2020-0600 Lot number: 2020-0600