Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
S-LIFT Slap Hammer Recalled by SpineFrontier, Inc. Due to Malfunction of slap hammer.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact SpineFrontier, Inc. directly.
Affected Products
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.
Quantity: 3
Why Was This Recalled?
Malfunction of slap hammer.
Where Was This Sold?
This product was distributed to 2 states: KS, TX
About SpineFrontier, Inc.
SpineFrontier, Inc. has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report