Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-1326-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

5/10 mm Weck Vista Universal Cannula, Catalog No. 405910RC; 5/10/12 mm Weck Vista Universal Cannula, Catalog No. 405912RC. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.

Product Classification:

Class II

Date Initiated: March 11, 2014

Date Posted: April 9, 2014

Recall Number: Z-1326-2014

Event ID: 67819

Reason for Recall:

Complaints of leakage of insufflation gas through the device.

Status: Terminated

Product Quantity: 55,521 total

Code Information:

Lots - Catalog No. 405910RC - 01J1200010, 01J1200242, 01K1200070, 01A1300141, 01B1300052, 01D1300319; Catalog No. 405912RC - 01G1200244, 01M1200020, 01M1200068, 01A1300546, 01A1300559

Distribution Pattern:

Worldwide Distribution-USA (nationwide) including Puerto Rico and the states of AL, AZ, AR, CA, CO, CT, FL, GA, IL, IN, KS, KY, MD, MA, MI, MN, MS, MO, NH, NJ, NY, NC, ND, OH, OR, PA, SC, TN, UT, VA, WA, WV, WI and the countries of Australia, Brazil, Canada, China, Israel, Korea, Malaysia, Singapore, and Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated