SpineFrontier, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1870-2013)

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:

S-LIFT Slap Hammer, Part Number: 11-50204, Revision A The slap hammers are used primarily to remove trial instruments that are used to estimate sizes of intervertebral body fusion devices intended to promote fusion. These devices were used in conjunction with lumbar intervertebral body fusion device intended for intervertebral body fusion of the spine of skeletally mature patients.

Product Classification:

Class II

Date Initiated: April 25, 2013

Date Posted: August 7, 2013

Recall Number: Z-1870-2013

Event ID: 65033

Reason for Recall:

Malfunction of slap hammer.

Status: Terminated

Product Quantity: 3

Code Information:

Lot: 56H26

Distribution Pattern:

US distributions to states of: KS and TX.

Voluntary or Mandated:

Voluntary: Firm initiated