Z-1870-2013 Class II Terminated
FDA device recall Z-1870-2013 was initiated by SpineFrontier, Inc. on Apr 25, 2013 and is designated Class II. Reason for recall: Malfunction of slap hammer. The recall status is terminated (terminated Jan 9, 2014). Affected quantity: 3.
Recall details
- Product Type
- Devices
- Report Date
- Aug 7, 2013
- Initiation Date
- Apr 25, 2013
- Termination Date
- Jan 9, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3
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.
Reason for recall
Malfunction of slap hammer.
Distribution pattern
US distributions to states of: KS and TX.
Code information
Lot: 56H26
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1870-2013
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026