Orthopedic Alliance LLC

Complete recall history across all FDA and CPSC categories — 10 total recalls

Orthopedic Alliance 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 (10)

FDA medical device enforcement actions by Orthopedic Alliance LLC

Date Product Reason Class
Mar 7, 2013 Orthopedic Alliance Spine System (alias "Blue & Gold") Part Numbers: BG... Orthopedic Alliance is recalling Blue & Gold Implants and Instruments because... Class II
Feb 20, 2013 Femoral component, CR, cemented, #1, left 2103-1310 Femoral component, CR, c... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Femoral head, standard, ¿26mm, +0mm Femoral head,medium, ¿26mm,+3mm Femoral... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Bipolar Cap, ID26mm, OD42mm Bipolar Cap, ID28mm, OD44mm Bipolar Cap, ID28mm... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Co-Cr cancellous bone screw,15mm Co-Cr cancellous bone screw,20mm Co-Cr can... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Ball Head, 28 Short CERAMIC Ball Head, 28 Medium CERAMIC Ball Head, 28 Long... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Zweimueller Type Stem SCS-Standard Sz 01 Zweimueller Type Stem SCS-Standard ... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 U2 Acetabular cup, Ti beads porous coated, ¿44mm U2 Acetabular cup, Ti beads... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 Tibial baseplate,cemented,#1 2203-3010 Tibial baseplate,cemented,#2 2203-302... The recall of the Loaner Bin and Sterilization Trays for implants and instrum... Class II
Feb 20, 2013 UKNEE Patella,small 2401-1010 UKNEE Patella,medium 2401-1020 UKNEE Patella,... 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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