Spinal Solutions, LLC

Complete recall history across all FDA and CPSC categories — 11 total recalls

Spinal Solutions, LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (11)

FDA medical device enforcement actions by Spinal Solutions, LLC

Date Product Reason Class
Mar 8, 2013 APLIF Implants and Instruments, Part Numbers: 184008-10 Anterior Psoas L... Spinal Solutions is recalling the APLIF system because it is not supported by... Class II
Feb 20, 2013 60 mm Rod, Item #BG1660 Product Usage: Spinal Solutions distributes a var... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 50 mm Screw, Item #BG7050 Product Usage: Spinal Solutions distributes a v... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 50 mm Rod, Item #BG1650 Product Usage: Spinal Solutions distributes a var... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 40 mm Rod, Item #BG1640 Product Usage: Spinal Solutions distributes a var... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Copperhead IBFD, Large Neutral, 6mm Copperhead IBFD, Large Neutral, 7mm C... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 12mm x 27mm x 8mm 12mm x 27mm x 9mm 12mm x 27mm x 10mm 12mm x 27mm x 11... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 14 x 11 x 6mm 7 deg 14 x 11 x 7mm 7 deg 14 x 11 x 8mm 7 deg 14 x 11 x 9... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Fang Screw 20mm Fang Plate 21mm Product Usage: Spinal Solutions distrib... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Set Screw, Item #BG3010 Product Usage: Spinal Solutions distributes a var... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 45 mm Screw, Item #BG7045 Product Usage: Spinal Solutions distributes a v... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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