Z-1282-2018 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- April 11, 2018
- Initiation Date
- October 26, 2017
- Termination Date
- December 10, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 50,263
Product Description
Radial Artery Catheterization Kit; Model: AK-04020
Reason for Recall
The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
Distribution Pattern
US nationwide distribution, including Puerto Rico.
Code Information
Lots: 13F16H0263, 13F16J0335, 13F16K0145, 13F16M0246, 13F17C0500, 13F17F0199, 13F17F0473, 13F17F0530, 13F17G0325, 23F16E1189, 23F16E1190, 23F16F0474, 23F16F1041, 23F16H0164; Expiration dates: October 2018 through March 2020