Cook Medical Recalls Zilver 635 Biliary Stent for Incorrect Instructions
Cook Medical is recalling Zilver 635 Biliary Stents because the instructions for use contain incorrect details regarding the removal of the delivery system.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a documentation error (incorrect instructions) rather than a physical defect or reported injury, fitting the 'Moderate' criteria for minor labeling or documentation issues.
Plain-English summary
Cook Medical Incorporated is recalling 9,834 units of the Zilver 635 Biliary Stent 5mm x 80mm (Catalog Number: ZIB6-125-5.0-80). The recall is due to an error in the instruction for use (IFU) document. Specifically, the instructions provided for the removal of the delivery system during the deployment of the stent are incorrect.
The affected stents are intended for the palliation of malignant neoplasms in the biliary tree. The recall covers units distributed nationwide across the United States, including all 50 states, the District of Columbia, and Puerto Rico.
The FDA has classified this recall as Class II. The manufacturer is correcting the IFU to amend the incorrect instruction details. No specific consumer action is detailed in the source text beyond the correction of the documentation.
The recalled product
- Product
- Zilver 635 Biliary Stent 5mm x 80mm, Catalog Number: ZIB6-125-5.0-80 Product Usage: The Zilver 518 and 635 Biliary Stents are intended for palliation of malignant neoplasms in the biliary tree.
- Manufacturer
- Cook Medical Incorporated
- Category
- Medical Device — Biliary Stent
- Hazard
- Affected units
- 9,834
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- GPN: G36022
Distribution
Part of a larger recall action
This product is one of 39 recalled by Cook Medical Incorporated under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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