Compass Health Brands (Corporate Office)

Complete recall history across all FDA and CPSC categories — 9 total recalls

Compass Health Brands (Corporate Office) 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 (9)

FDA medical device enforcement actions by Compass Health Brands (Corporate Office)

Date Product Reason Class
Mar 7, 2023 REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Inten... Error in the Introduction section of the user manual that indicates the devic... Class II
Jan 10, 2022 Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx (RLE... Wheel spoke may crack causing the wheel to separate from the axle may result ... Class II
Apr 8, 2019 MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, ... Product design change did not receive proper premarket clearance and lacks a ... Class II
Apr 8, 2019 MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, M... Product design change did not receive proper premarket clearance and lacks a ... Class II
Apr 8, 2019 MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Mo... Product design change did not receive proper premarket clearance and lacks a ... Class II
Apr 8, 2019 MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, ... Product design change did not receive proper premarket clearance and lacks a ... Class II
Apr 8, 2019 MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient, M... Product design change did not receive proper premarket clearance and lacks a ... Class II
Apr 8, 2019 MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #... Product design change did not receive proper premarket clearance and lacks a ... Class II
Jun 18, 2018 CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L ... A May 2015 design change in the cushion seal replacement part and accompanyin... Class I

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.