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SpineFrontier, Inc. recalls S-LIFT Slap Hammer, Part Number: 11-50204, Revision A The slap hammers are used primarily to remove trial instruments
Recalled August 7, 2013 · FDA recall Z-1870-2013 · SpineFrontier
Hazard
Malfunction of slap hammer. · FDA Class II
Units
3
Sold at
US distributions to states of: KS and TX.
Description
Malfunction of slap hammer.
Product
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.
Manufacturer(s)
SpineFrontier, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →