CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit. 2 units per case The devices could be branded as Halyard Health.
FDA Recall Z-0370-2020 · Posted None
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Recalling FirmAvanos Medical, Inc.
Recall StatusTerminated
Product CodeKNT
Date Initiated2019-10-08
Date Terminated2022-03-16
Product Quantity104 cases (208 units) total
Reason for Recall
The connector piece to the PEG tube does not pass over the guidewire.
Firm Action
Avanos Medical notified customers of the recall on about 10/08/2019, via "URGENT: PRODUCT RECALL" letter. Customers were informed that there is a potential where the PEG tube does not pass over the guidewire.
Instructions included to evaluate your inventory for any affected products, discontinue use of any affected product, quarantine any on hand, and arranged for the return of affected product. Customers were also instructed to complete the provide Recall Acknowledgement Form (Attachment 1) and return a copy of the form to Avanos in the USA by email to [email protected] or by FAX to 1-888-807-1084. Outside the USA, please send by email to [email protected] or by FAX to +44 (0) 20 7660 1462.
For further assistance, please contact Avanos by email at [email protected] or by FAX to 1-888-807-1084. Outside the USA, please send by email to [email protected] or by FAX to +44 (0) 20 7660 1462. You may also contact Avanos Customer Service at [email protected].
Root Cause
Under Investigation by firm
Distribution Pattern
Distribution to CT, IN, MD, NJ, PA, VA. International distribution to Great Britain.
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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