Davol, Inc., Sub. C. R. Bard, Inc. Davol Salute Reusable 18cm Shaft (Short/Open) Item Numbers: 0113037-Product Code: 9113037(Refurbished) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Davol Salute Reusable 18cm Shaft (Short/Open) Item Numbers: 0113037-Product Code: 9113037(Refurbished)
Brand
Davol, Inc., Sub. C. R. Bard, Inc.
Lot Codes / Batch Numbers
All serial numbers
Products Sold
All serial numbers
Davol, Inc., Sub. C. R. Bard, Inc. is recalling Davol Salute Reusable 18cm Shaft (Short/Open) Item Numbers: 0113037-Product Code: 9113037(Refurbishe due to Malformed constructs (straight shots) may form causing injury to user/patient. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Malformed constructs (straight shots) may form causing injury to user/patient
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026