Atlas FDA

Smith & Nephew Endoscopic Disposable Blades:TURBOWHISKER BLD,EP-1,4.5MM(6) Part #: 7205316. DYONICS Series 3000 BONECUTT

FDA device recall Z-1567-2009 · posted 2009-07-14 · Terminated

Recall details

Recalling firm
Smith & Nephew, Inc. Endoscopy Division
Reason for recall
Product sterility is compromised due to breach in the sterile packaging.
Action taken
Smith & Nephew, Inc. issued a notification letter dated May 5, 2009 via Federal Express to User Facility and/or Sales Representatives on May 7, 2009 and an Email was sent to Sales Representatives. Accounts were requested to 1)complete the form and fax to Smith & Nephew, Inc. at 1-508-261-3636 and 2) return (using the firm's return authorization number) affected product to Smith & Nephew, Inc. Direct questions about this recall to Smith & Nephew, Inc. by calling 1-508-261-3655.
Root cause
Pending
Status
Terminated
Product code
NBH
Quantity affected
948 units
Distribution
Worldwide Distribution -- US, Switzerland, Canada, United Arab Emerites, Belgium, Mexico, South Africa, Great Britain, Australia, Korea, Japan, Germany, Israel, India, Taiwan, Greece, Italy, Turkey an
Date initiated
2009-05-07
Date posted
2009-07-14
Date terminated
2012-05-08
Location
Andover, MA

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