Z-0730-2019 Class II Terminated
FDA device recall Z-0730-2019 was initiated by Smith & Nephew, Inc. on January 7, 2019 and is designated Class II. Reason for recall: The pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble. The recall status is terminated (terminated September 17, 2020). Affected quantity: 72 units.
Recall Details
- Product Type
- Devices
- Report Date
- January 23, 2019
- Initiation Date
- January 7, 2019
- Termination Date
- September 17, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 72 units
Product Description
SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613
Reason for Recall
The pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble.
Distribution Pattern
NY, TN, Germany, Italy, Great Britain, Singapore
Code Information
Lot Numbers: C63165, C63306, C63495