Etac Supply Center Ab

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

Etac Supply Center Ab 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 Etac Supply Center Ab

Date Product Reason Class
Jul 12, 2015 Etac Relax wall mounted shower seat The Etac Relax is a wall mounted shower ... The recalling firm has received reports of a malfunction of the Relax wall mo... Class II
Jun 15, 2015 Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable an... The Supporter toilet armrest has two Fast Nuts fixing the product to the toil... Class II
May 23, 2013 Swift Mobil shower chair, Swift Mobil 160 shower chair, and Swift Mobil Tilt ... Etac is voluntarily conducting a field correction of the Etac Swift Mobil sho... Class II
Apr 6, 2012 Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker. These produ... The recall has been initiated because there is the potential that users may f... 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.

Explore More Recalls

Search recalls by category, state, reason, or firm across all our databases.