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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:117721

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.

Official recall number

Z-1870-2013

Evidence summary

Product code
FZY
Recall status
Terminated
Event initiated
April 25, 2013
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1870-2013

Field note

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