Stryker Sustainability Solutions: Medical Device Recall in 2017 - (Recall #: Z-0272-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector. Intended for use in preventing deep vein thrombosis (DVT), diminishing post-operative pain and swelling, enhancing blood circulation and reducing wound healing time on the calf.

Product Classification:

Class II

Date Initiated: December 1, 2017

Date Posted: December 27, 2017

Recall Number: Z-0272-2018

Event ID: 78714

Reason for Recall:

3040 compression sleeves being mislabeled as a 3010-PL compression sleeves.

Status: Terminated

Product Quantity: 280 devices

Code Information:

Lot 6285035. UDI: 00885825016661.

Distribution Pattern:

Distributed to Texas.

Voluntary or Mandated:

Voluntary: Firm initiated