RecallRadar

FDA Device recall Z-1277-2014

10mm Weck¿ Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to provide access, illuminat…

On 2014-04-02 the FDA classified a Class II recall of 10mm Weck¿ Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to provide access, illuminat… by Teleflex Medical, citing complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1277-2014
ClassificationClass II
Statusterminated
Initiated2014-03-11
Published2014-04-02
Last updated2026-09-13 11:53 UTC
CompanyTeleflex Medical
DistributionUS

Product

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.

Reason

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

Identifiers

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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1277-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.