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All product recalls associated with Spinal Concepts, Inc.
Total Recalls
4
Past Year
0
Class I (Serious)
0
Most Recent
Apr 2004
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Handle becomes loose after repeated use.
Recall of product literature that describes use of the device.
Design has insufficient articulating distance between the two component plates to prevent disassociation in vivo.
Design has insufficient articulating distance between the two component plates to prevent disassociation in vivo.