Atlas FDA

Davol Salute Fixation Reusable Handle Item Code: 0113024-Product Code 9113024 (Refurbished)

FDA device recall Z-1266-2007 · posted 2007-09-27 · Terminated

Recall details

Recalling firm
Davol, Inc., Sub. C. R. Bard, Inc.
Reason for recall
Malformed constructs (straight shots) may form causing injury to user/patient
Action taken
Davol issued recall letter notification on 7/16/07 via Federal Express. Sales of the disposable cartridges ceased July 31, 2007. Cartridges will not be requested to be returned to Davol. Customer requests to return cartridges will be managed on an account-by-account basis. A reminder Second Letter issued July 23,2007 as a follow-up to the letter of July 16, 2007. The second stage will be a series of three letters to customers following the cessation of disposable cartridge sales and to recall the re-usable handles. A Stock Status form will be provided to customers to inventory the product which they are returning. The Stock Status form will be used to document the handles being returned. In the event that the customer cannot locate one or more handles. All handles will be returned to Cranston and will be dispositioned. Account verification for the number of handles returned from the account will be performed. No verification testing will be performed on returned handles unless a formal complaint has been registered for a handle.
Root cause
Device Design
Status
Terminated
Product code
GDW
Quantity affected
5,268 handles
Distribution
Worldwide-USA and Canada, Austria, Switzerland, Spain, Sweden, United Kingdom, Italy,Portugal, Greece,Holland, South Africa, Israel, Japan, Belgium, Denmark, Finland, France, and Germany
Date initiated
2007-07-16
Date posted
2007-09-27
Date terminated
2018-08-16
Location
Cranston, RI

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Related 510(k) clearances

RecordFirmDate
SALUTE FIXATION SYSTEM (K050610)Davol Inc., Sub. C. R. Bard, Inc.2005-05-25