Z-1244-2017 Class II Terminated
FDA device recall Z-1244-2017 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: 1410.
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
- 1410
Product Description
Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706
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: 50439354 50393992 50252777 50208023 50171402 50138054 50103142 50066114 576304