The Recall Desk

Manufacturer

Compass Health Brands (Corporate Office)

9 recalls in our database name Compass Health Brands (Corporate Office) as the manufacturing or recalling firm.

What the numbers show

Total
9
Critical
0
Severe
0
Most recent
2023-04-26

Of the 9 recalls from Compass Health Brands (Corporate Office) we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–9 of 9

  • ModerateFDA (Devices)·Z-1398-2023·2023-04-26

    Pressure Therapy System Recalled for Unauthorized Deep Vein Thrombosis Prevention Claim

    Compass Health Brands is recalling the REX Pressure Therapy System because the user manual incorrectly claims the device can prevent deep vein thrombosis, an indication for which the device was not FDA-cleared.

    Product
    REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. Models: DVTREX-U and DVTREX -L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0510-2022·2022-01-26

    Voyager Rollator Walkers Recalled for Wheel Separation and Fall Risk

    Compass Health Brands is recalling 3,734 Voyager Rollator walkers due to cracking wheel spokes that may cause wheels to separate from the axle, potentially resulting in patient falls and injuries.

    Product
    Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx (RLEU10BL, RLEU10PK, RLEU10WT) RLEU10BL Voyager Rollator Cobalt Blue UPC: 815067078066; RLEU10PK Voyager Rollator Rose Gold UPC: 815067078073; RLEU10WT Voyager Rollator Ice Palace UPC: 815067078080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1348-2019·2019-05-22

    MediPress Pneumatic Compression System Recalled for Lack of Clearance

    Compass Health Brands is recalling MediPress pneumatic compression systems because a design change lacked proper FDA premarket clearance.

    Product
    MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, Model #6104S-S
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1343-2019·2019-05-22

    MediPress Pneumatic Compression System Recalled for Missing Premarket Clearance

    Compass Health Brands is recalling the MediPress pneumatic compression system because a design change lacked proper FDA premarket clearance.

    Product
    MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1347-2019·2019-05-22

    MediPress Pneumatic Compression System Recalled for Lack of Clearance

    Compass Health Brands is recalling MediPress pneumatic compression systems because a design change lacked proper FDA premarket clearance.

    Product
    MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient, Model #6103S-S
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1344-2019·2019-05-22

    MediPress Pneumatic Compression System Recalled for Lack of Clearance

    Compass Health Brands is recalling MediPress pneumatic compression systems because a design change lacked proper FDA premarket clearance.

    Product
    MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, Model #6103M-S
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1345-2019·2019-05-22

    MediPress Pneumatic Compression System Recalled for Missing Premarket Clearance

    Compass Health Brands is recalling MediPress pneumatic compression systems because a product design change lacked proper FDA premarket clearance.

    Product
    MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model #6104M-S
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-1346-2019·2019-05-22

    MediPress Pneumatic Compression System Recalled for Lack of Clearance

    Compass Health Brands is recalling MediPress pneumatic compression systems because a design change lacked proper FDA premarket clearance.

    Product
    MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Model #6103L-S
    Category
    Medical Device
    Distribution
    36 states
  • HighFDA (Devices)·Z-2741-2018·2018-08-29

    Compass Health Brands Recalls CPAP Mask Cushions Due to Design Incompatibility

    Compass Health Brands is recalling CPAP mask cushions because a design change makes them incompatible with previous elbow parts, potentially causing unacceptable CO2 porting.

    Product
    CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L Product Usage: A CPAP mask is attached to an end user s face and a CPAP machine, to treat end users with sleep apnea. The replacement cushion is a non-durable component that requires replacement every 3
    Category
    Medical Device
    Distribution
    Distributed nationwide