Recall StatusTerminated
Date Initiated2016-11-16
Date Terminated2019-08-19
Product Quantity4444 units
Reason for Recall
The firm received complaints of cracks in the weld on the head of the mallet. In the reported cases, some of the lead beads and particles escaped from the mallet into the surgical wound.
Firm Action
Smith and Nephew sent an Urgent - Product Recall 1 st Notification dated November 16, 2016, to all affected customers.
Actions for Hospital Representatives:
1. Please inspect your inventory and locate any unused devices from the above listed product and batch numbers, and quarantine them immediately.
2. Complete the last two columns in the Inventory Return Certification Form on the following page, indicating the quantities
that need to be returned. If you do not have product to return, please place an x in the column No Product to Return. Include your contact information in the spaces provided at the bottom of the form.
3. Please contact Smith & Nephews Field Actions Department via email at
[email protected] or fax +1- 901-566-7975 to return the completed Inventory Return Certification Form and obtain a return authorization (RA) number if you have product to return.
4. Return any affected product to the address listed on the Inventory Return Certification Form. Please indicate the RA number on your return shipment.
Actions for Smith & Nephew Affiliates/Distributors
1.Send this letter to your customers and ask them to return the recalled product.
2. Please inspect your inventory and locate any unused devices from the above listed product and batch numbers, cease distribution and use of those products, and quarantine them immediately.
3. Complete the last two columns in the Inventory Return Certification Form above, indicating the quantities that need to be returned. If you do not have product to return, please place an x in the column No Product to Return. Include your contact information in the spaces provided at the bottom of the form.
4. Please contact Smith & Nephews Field Actions Department via email at
[email protected] or fax +1- 901-566-7975 to return the completed Inventory Return Certification Form and obtain a return authorization (RA) number if you have product to return.
5. Return any affected product
Root Cause
Process control
Distribution Pattern
Worldwide Distribution - USA (nationwide) Distribution including Puerto Rico and to the countries of : Argentina, Austria, Australia, Belgium, Bahrain, Brazil, Canada, China, Colombia, Costa Rica, Dubai, Denmark, Germany, Finland, France, Great Britain, Greece, Hong Kong, Ireland, Israel, India, Italy, Japan, Mexico, Malaysia, Netherlands, Norway, Poland, Portugal, Puerto Rico, South Africa, Sweden, Singapore, Switzerland, Thailand, Turkey and Venezuela.
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.