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Terminated

Flex-Neck Classic Peritoneal Dialysis Catheter 1 Cuff Infant Coiled, Catalog # CF-4235/B

FDA Recall Z-1143-2018 · Posted None

Recall StatusTerminated
Product CodeFJS
Date Initiated2017-09-20
Product Quantity30

Reason for Recall

2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product.

Firm Action

On 09/20/17, an URGENT PRODUCT RECALL NOTICE was sent to all direct consignees via mail, informing them of a voluntary recall of specific lots of peritoneal dialysis catheters and catheter containing kits. Consignees were advised to immediately do the following: identify and quarantine effected devices; inform personnel to whom the devices were distributed of the field action; fill out and email the customer response form to [email protected] within 5 days, and return effected devices within ten days using Federal Express account 112952756. Consignee questions were directed to phone: 801-208-4381 or fax: 801-316-4880. Sales representatives were sent an email communication informing them of the recall and instructing them to contact effected customers to help them return Customer Response Forms and product.

Root Cause

Mixed-up of materials/components

Distribution Pattern

United States, Austria, Finland, Germany, Ireland, Switzerland, and United Kingdom

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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