Medical Vision Ab: Medical Device Recall in 2016 - (Recall #: Z-2705-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures.

Product Classification:

Class II

Date Initiated: May 10, 2016

Date Posted: September 7, 2016

Recall Number: Z-2705-2016

Event ID: 74190

Reason for Recall:

Sterility of device may be compromised due to sterile package breakage.

Status: Terminated

Product Quantity: 3,295 devices

Code Information:

All lot numbers of Double Pump RF Patient Cassettes delivered to the US, Batch numbers: 13I03, 14A01, 14A06, 14A09, 14A10, 14B03, 14B09, 14C06, 14C10, 14D07, 14D11, 14E06, 14E10, 14F01, 14F02, 14F03, 14F04, 14F10, 14F11, 14G07, 14H02, 14H04, 14H08, 14H09, 14J01, 14J02, and 14J03.

Distribution Pattern:

Distributed to the US, to the states of NH, OK, AL, PA, IL, MA, TX, MI, NC, CA, MN, CT, GA, NY, WI, KY, OH, VA, AL, NJ, TN, SD, and IN.

Voluntary or Mandated:

Voluntary: Firm initiated