Z-1424-2018 Class II Terminated
FDA device recall Z-1424-2018 was initiated by Carefusion 2200 Inc on February 23, 2017 and is designated Class II. Reason for recall: The integrity of the sterile packaging is potentially compromised. The recall status is terminated (terminated July 9, 2019).
Recall Details
- Product Type
- Devices
- Report Date
- April 25, 2018
- Initiation Date
- February 23, 2017
- Termination Date
- July 9, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
Product Description
JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 4, d.) 8G x 6, e.) 11G x 6]; STERILE;
Reason for Recall
The integrity of the sterile packaging is potentially compromised.
Distribution Pattern
Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam
Code Information
Product Code: a.) TJC3513 / LOT 0000848831, 0000851431, 0000854856; Product Code: b.) TJC4008 / LOT 0000841227, 0000846706, 0000848560, 0000849684, 0000853455; c.) TJC4011 / LOT 0000840667, 0000841228, 0000845874, 0000849717, 0000850937, 0000852121; d.) TJC6008 / LOT 0000841216, 0000848569, 0000851432, 0000852122, 0000853458; e.) TJC6011 / LOT 0000841124, 0000848571, 0000853975