Z-1239-2017 Class II Terminated
FDA device recall Z-1239-2017 was initiated by Smith & Nephew, Inc. on February 2, 2017 and is designated Class II. Reason for recall: The single use devices are provided sterile and do not have an expiration date on the label. The recall status is terminated (terminated September 20, 2019). Affected quantity: 2646.
Recall Details
- Product Type
- Devices
- Report Date
- March 1, 2017
- Initiation Date
- February 2, 2017
- Termination Date
- September 20, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2646
Product Description
Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
Reason for Recall
The single use devices are provided sterile and do not have an expiration date on the label.
Distribution Pattern
Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela
Code Information
Batch Numbers: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 50158655 50138049 50119457 50089297 50082581 50069485