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AAP Implantate Ag

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

AAP Implantate Ag 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 AAP Implantate Ag

Date Product Reason Class
Nov 28, 2019 aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00 The company has become aware that the soft tissue retractor is not always rem... Class II
Jan 25, 2019 INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425 Products were distributed with the incorrect instructions for use. Class III
Jan 25, 2019 INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453 Products were distributed with the incorrect instructions for use. Class III
Jan 11, 2019 aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Su... There is the potential for the Lambotte chisel to break at the welded piece 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.

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