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Signature Orthopedics Pty Limited

Complete recall history across all FDA and CPSC categories — 4 total recalls

Signature Orthopedics Pty Limited 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 (4)

FDA medical device enforcement actions by Signature Orthopedics Pty Limited

Date Product Reason Class
Apr 20, 2021 Logical cup liner - Product Usage: intended to replace a hip joint where bone... Product mislabeled, with the incorrect product inside the package. Class II
Dec 10, 2018 Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement... Product mix up Class II
Dec 10, 2018 Genius Knee Cemented Tibial Component Product Usage: Knee replacement com... Product mix up Class II
Feb 2, 2018 Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature cer... This recall has been identified due to the batch being mislabeled, with the p... 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.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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