Securitas Healthcare LLC

Complete recall history across all FDA and CPSC categories — 10 total recalls

Securitas Healthcare LLC 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 (10)

FDA medical device enforcement actions by Securitas Healthcare LLC

Date Product Reason Class
Dec 8, 2025 Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1... Securitas Healthcare has become aware of a firmware issue in the Call Station... Class II
Dec 8, 2025 Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version:... Securitas Healthcare has become aware of a firmware issue in the Call Station... Class II
Nov 1, 2024 Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjuncti... Certain software versions will not notify end users of calls initiated by cal... Class II
Jun 20, 2024 Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireles... This is a risk that alarms will not be received by the Arial Wireless Nurse C... Class II
Jun 20, 2024 Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery... There is a risk that alarms will not be received by the Arial Wireless Emerge... Class II
Apr 11, 2024 Arial mobile application, model numbers 54640, 54630, and 54630-SMA, that ut... The Arial Mobile Application utilizing Apple iOS 17.4 and iOS 17.5 is freque... Class II
Sep 25, 2023 Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-5936... Premature battery depletion presents a risk that alarms will not be received ... Class II
Sep 25, 2023 Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; ... Premature battery depletion presents a risk that alarms will not be received ... Class II
Sep 25, 2023 Arial Water Resistant Pendant with Long Wristband, Models: 59362 and 2560-59... Premature battery depletion presents a risk that alarms will not be received ... Class II
Feb 6, 2023 Arial mobile application, model #54630 and #54640 for Android devices downloa... The mobile application for Android devices downloaded from the Google Play St... 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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