Reported May 22, 2019 · Terminated

MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S

Compass Health Brands (Corporate Office)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Compass Health Brands (Corporate Office) · 6753 Engle Rd · Middleburg Heights, OH · 44130-7934

Is this the product you have?

  • MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Lot codes and dates
  • All Serial Numbers/Lots

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

Why it was recalled

Product design change did not receive proper premarket clearance and lacks a 510 (k)

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Compass Health Brands (Corporate Office) recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 26, 2020 · Data as of Sep 19, 4:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.