RecallRadar

FDA Device recall Z-1324-2014

10mm Weck Vista Cannula-only, Catalog No. 405910C, 12mm Weck Vista Cannula-only, Catalog No. 405912C. An endoscope and accessories is a dev…

On 2014-04-09 the FDA classified a Class II recall of 10mm Weck Vista Cannula-only, Catalog No. 405910C, 12mm Weck Vista Cannula-only, Catalog No. 405912C. An endoscope and accessories is a dev… by Teleflex Medical, citing complaints of leakage of insufflation gas through the device.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1324-2014
ClassificationClass II
Statusterminated
Initiated2014-03-11
Published2014-04-09
Last updated2026-09-13 11:53 UTC
CompanyTeleflex Medical
DistributionUS

Product

10mm Weck Vista Cannula-only, Catalog No. 405910C, 12mm Weck Vista Cannula-only, Catalog No. 405912C. 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 of leakage of insufflation gas through the device.

Identifiers

code_info
Lots - Catalog No. 405910C - 01G1200243, 01J1200226, 01L1200368, 01A1300177, 01D1300107, 01E1300140, 01E1300435, Catal…Lots - Catalog No. 405910C - 01G1200243, 01J1200226, 01L1200368, 01A1300177, 01D1300107, 01E1300140, 01E1300435, Catalog No. 405912C - 01J1200384, 01K1200725, 01L1200352, 01D1300319

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-1324-2014%22

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