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BARD Ventrio Small Circle Hernia Patch 3.0" Product Code: 0010213 Indicated for use in the reconstruction of soft tissue

FDA device recall Z-0424-2011 · posted 2010-11-19 · Terminated

Recall details

Recalling firm
Davol, Inc., Sub. C. R. Bard, Inc.
Reason for recall
Mislabeled: Hernia Patch may be a different size than on the product label
Action taken
Davol notified accounts by an Urgent: Medical Device Recall letter on 10/15/10 via overnight delivery. The letter stated that the product maybe a different size than indicated on the product label. It also identified the affected product. Accounts are requested to examine their inventory, remove, and return recalled product. Customers are to notify any of their customers that they may have further distributed the affected product to by including a copy of the recall notice. Customers should contact Davol Customer Service 1-800-556-6275 for instructions on how to return the affected product. Customers are also requested to complete and fax back the attached fax sheet to 1-401-825-8753. If there are any additional questions, customers should contact Davol Customer Service Department at 1-800-556-6275 or C.R. Bard's Medical Service Support Department at 1-800-562-0027.
Root cause
Packaging process control
Status
Terminated
Product code
FTL
Quantity affected
26 units
Distribution
Nationwide Distribution
Date initiated
2010-10-15
Date posted
2010-11-19
Date terminated
2011-10-27
Location
Warwick, RI

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Related 510(k) clearances

RecordFirmDate
VENTRIO HERNIA PATCH (K081777)C.R. Bard, Inc.2008-09-29