PlainRecalls
FDA Devices Moderate Class II Ongoing

Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 50-80mm Model/Catalog Number: MR2102050 Product Description: Cranial Caudal Blade Component: Yes, a component of a retractor blade

Reported: July 10, 2024 Initiated: May 17, 2024 #Z-2235-2024

Product Description

Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 50-80mm Model/Catalog Number: MR2102050 Product Description: Cranial Caudal Blade Component: Yes, a component of a retractor blade

Reason for Recall

Cranial Caudal Blades manufactured incorrectly could result in fracture and/or damage to the bone structure

Details

Units Affected
31 units
Distribution
United States Nationwide distribution in the states of Nevada, Texas, Michigan, Rhode Island, California, Oregon, Oklahoma, New York, Minnesota.
Location
Carlsbad, CA

Frequently Asked Questions

What product was recalled?
Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 50-80mm Model/Catalog Number: MR2102050 Product Description: Cranial Caudal Blade Component: Yes, a component of a retractor blade. Recalled by SEASPINE ORTHOPEDICS CORPORATION. Units affected: 31 units.
Why was this product recalled?
Cranial Caudal Blades manufactured incorrectly could result in fracture and/or damage to the bone structure
Which agency issued this recall?
This recall was issued by the FDA Devices on July 10, 2024. Severity: Moderate. Recall number: Z-2235-2024.