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Recall Observatory FDA recall evidence

Device product

MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Model #6103L-S

Z-1346-2019

April 08, 2019

Class II

Product summary

Firm
Compass Health Brands (Corporate Office)
Event
Event 82629
Status
Terminated
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-1346-2019

Official wording

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

Code information: All Serial Numbers/Lots

Distribution pattern: Domestically to AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TN, KY, TX, UT, VA, WA, WI & WY Internationally to Canada

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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