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Recall Observatory FDA recall evidence

Device product

Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for chronic, acute, traumatic, subacute, and dehisced wounds/ulcers/partial thickness burns/flaps/grafts.

Z-1041-2017

November 11, 2016

Class II

Product summary

Firm
Smith & Nephew, Inc.
Event
Event 75966
Status
Ongoing
Classification
Class II
Quantity
15,960 units in the US
Official record key
device-enforcement:Z-1041-2017

Official wording

Reason: Lack of 510k clearance for design modification.

Code information: Model No. 66800164; All pumps of this model are affected.

Distribution pattern: Nationwide

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Lack of 510k clearance for design modification.