Z-1241-2017 Class II Terminated
FDA device recall Z-1241-2017 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: 4500.
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
- 4500
Product Description
Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703
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: 50525150 50386077 50261802 50197616 50178740 50171398 50158656 50138050 50121538 50103379 50089298 50082582 50061131