Z-2274-2012 Class II Terminated
FDA device recall Z-2274-2012 was initiated by Atlas Spine, Inc. on June 4, 2009 and is designated Class II. Reason for recall: Atlas Spine, Inc. recalled their Apelo Modular Screwdriver, a component of the Apelo Pedicle Screw System Instrumentation, because of complaints received about the tip breaking. If the tip is fracture… The recall status is terminated (terminated July 16, 2014). Affected quantity: 4 pieces.
Recall Details
- Product Type
- Devices
- Report Date
- September 5, 2012
- Initiation Date
- June 4, 2009
- Termination Date
- July 16, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4 pieces
Product Description
Apelo Modular Screwdriver labeled in part: "APELO PEDICLE SCREW SYSTEM***Modular Screwdriver***Atlas Spine, Inc.***www.AtlasSpine.com*** 1555 Jupiter Park Drive #4***Jupiter, Florida 33458***561-741-1108***Tissue Sleeve***MFG Date: XX/XX/XXXX***Lot #: XXXX***Weldment***MFG Date: 03/23/2009***Sleeve Assembly***MFG Date: XX/XX/XXXX***Lot #: XXXX***Qty: 1 Rx Only***Non-Sterile. Sterilize Prior to Use*** Rev. A***. The Modular Screwdriver is used to insert modular pedicle screw implants which are part of the Apelo System.
Reason for Recall
Atlas Spine, Inc. recalled their Apelo Modular Screwdriver, a component of the Apelo Pedicle Screw System Instrumentation, because of complaints received about the tip breaking. If the tip is fractured inside of the modular screw, the tip could become implanted in the body or if the entire screw is removed, it could cause a delay in the surgery.
Distribution Pattern
USA Distribution to the state of Florida only.
Code Information
PN# 70175-001 CAT#2006-41-0000 Lot # 00686