SpineNet: Medical Device Recall in 2013 - (Recall #: Z-2107-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow.

Product Classification:

Class II

Date Initiated: February 4, 2013

Date Posted: September 4, 2013

Recall Number: Z-2107-2013

Event ID: 65914

Reason for Recall:

SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.

Status: Terminated

Product Quantity: 100 units

Code Information:

Lot # 22754F16 and #25854I17

Distribution Pattern:

Distributed to one customer in Florida.

Voluntary or Mandated:

Voluntary: Firm initiated