Data Foundry

Medical device recalls 2014

5/10 Weck Vista Universal Balloon Open Access Port — Class II medical device recall Z-1328-2014

Terminated recall by Teleflex Medical, reported 2014-04-09, distributed nationwide. Complaints of leakage of insufflation gas through the device.

Recall numberZ-1328-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTeleflex Medical, Durham, NC, United States
Recall initiated2014-03-11
Classified2014-04-02
Reported by FDA2014-04-09
Terminated2016-01-28
DistributedNationwide (US)
Countries outside the USAU, BR, CA, CN, IL, KR, MY, SG, VN
Quantity55,521 total
Reason classespackaging
Model numbers01A1300178, 01A1300202, 01A1300203, 01D1300316, 01D1300412, 01E1300137, 01E1300310, 01E1300436, 01J1200219, 01J1200231, 01J1200241, 01K1200066, 01K1200067, 01K1200597, 01K1200600, 01K1200601, 01K1200618, 01K1200619, 01K1200622, 01K1200623, 01K1200728, 01L1200056, 01L1200354, 01L1200355, 01L1200378 and 8 more

Product

5/10 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm), Catalog No. 410944, 5/10 Weck Vista Universal Balloon Open Access Port - Long Length (100mm), Catalog No. 410944L; 5/10 Weck Vista Universal Balloon Open Access Port - Short Length (53mm), Catalog No. 410944S; 5/10/12 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm), Catalog No. 412944; 5/10/12 Weck Vista Universal Balloon Open Access Port - Long Length (100 mm), Catalog No. 412944L. 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 for recall

Complaints of leakage of insufflation gas through the device.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1328-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.