10mm Weck Vista Cannula-only, Catalog No. 405910C, 12mm… recallZ-1324-2014 · Teleflex Medical · initiated Mar 11, 2014
Class II Terminated All recalls posted in April 2014
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Teleflex Medical or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Complaints of leakage of insufflation gas through the device.
FDA root cause category: Nonconforming Material/Component
What the company is doing
Letters were issued on March 11, 2014 to customers informing them of the recall. The letter asked the consignee to immediately discontinue use and quarantine any products on hand. The letter included a Recall Acknowledgement Form which is to be returned. A letter was also issued to distributors on March 11, 2014, requesting them to conduct a sub-recall.
Recall details
- Recall number
- Z-1324-2014
- Recall class
- Class II
- Status
- Terminated
- Initiated by the company
- Mar 11, 2014
- Posted by the FDA
- Apr 2, 2014
- Recalling firm
- Teleflex Medical
- Quantity
- 55,521 total
- Product code
- GCJ
- FDA submissions
- K121796
- Distribution
- 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.
Product description
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.
Code information (models, lots, serial numbers)
Lots - Catalog No. 405910C - 01G1200243, 01J1200226, 01L1200368, 01A1300177, 01D1300107, 01E1300140, 01E1300435, Catalog No. 405912C - 01J1200384, 01K1200725, 01L1200352, 01D1300319
Other devices under the same FDA submission
2 devices cleared under K121796 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- TAUT IPN914249Teleflex Incorporated · Laparoscope, general & plastic surgery9 reports
- TAUT IPN006689Teleflex Incorporated · Laparoscope, general & plastic surgery7 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 67819).
- Z-1326-2014 · Terminated5/10 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…
- Z-1328-2014 · Terminated5/10 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 N…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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