Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-1277-2014)

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:

10mm Weck¿ Vista" Cannula-only, Teleflex Medical, Product Usage: 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 2, 2014

Recall Number: Z-1277-2014

Event ID: 67710

Reason for Recall:

Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.

Status: Terminated

Product Quantity: 55,521 ea. in total

Code Information:

Product Code: 405912, Lot Number: 01J1200462, 01K1200129, 01K1200377, 01K1200596, 01K1200611, 01L1200369, 01A1300106, 01E1300218, 01E1300311, 01F1300135, and 01F1300079.

Distribution Pattern:

Worldwide Distribution - USA Nationwide including Puerto Rica and the countries of: Australia, Brazil, China, Canada, Malaysia, Korea, Ireland Singapore and Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated