Corflex
Complete recall history across all FDA and CPSC categories — 7 total recalls
Corflex 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 (7)
FDA medical device enforcement actions by Corflex
| Date | Product | Reason | Class |
|---|---|---|---|
| Nov 12, 2015 | ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075 Post-Op... | Knee brace could fail to maintain the locked position and a loss of balance ... | Class II |
| Nov 12, 2015 | HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operativ... | Knee brace could fail to maintain the locked position and a loss of balance ... | Class II |
| Nov 12, 2015 | CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Opera... | Knee brace could fail to maintain the locked position and a loss of balance ... | Class II |
| Nov 12, 2015 | ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231 Post-Operati... | Knee brace could fail to maintain the locked position and a loss of balance ... | Class II |
| Nov 12, 2015 | Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative... | Knee brace could fail to maintain the locked position and a loss of balance ... | Class II |
| Nov 12, 2015 | BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087 Post-O... | Knee brace could fail to maintain the locked position and a loss of balance ... | Class II |
| Nov 12, 2015 | CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Kn... | Knee brace could fail to maintain the locked position and a loss of balance ... | 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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