R82 A/S

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

R82 A/S 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 R82 A/S

Date Product Reason Class
Dec 8, 2021 R82 by ETAC Push Brace for High-Low The chrome surface of the push brace can crack during use, potentially cuttin... Class II
Mar 6, 2020 Chest Support for R82 Mustang, Model Numbers: 861810, 861820, 861830; and Ra... The plastic plug on the chest support for Mustang and Rabbit/Rabbit Up can co... Class II
Mar 28, 2019 Wombat Living, Size 3, Item Numbers: 953121-00, 953126-00, 953131-00, 9531... Firm received feedback form the market regarding breakage of the plastic join... Class II
Jun 30, 2017 Heron toilet and bath chair Model 880505-01 & 880505-11 Replacement campaign on all units that have a gas spring head in aluminum. 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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