Z-1908-2016 Class I Terminated
FDA device recall Z-1908-2016 was initiated by Hummingbird Med on March 11, 2015 and is designated Class I. Reason for recall: Hummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of insertion difficulties. The recall status is terminated (terminated February 7, 2017). Affected quantity: 62,400.
Recall Details
- Product Type
- Devices
- Report Date
- July 13, 2016
- Initiation Date
- March 11, 2015
- Termination Date
- February 7, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 62,400
Product Description
ABG-HM-1 Hummi Micro Draw Blood Transfer Device; Used for blood transfer and collection from peripheral arterial line catheters.
Reason for Recall
Hummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of insertion difficulties.
Distribution Pattern
US Distribution in the state of CA.
Code Information
Lot Numbers: 20140510 20140513 20140516 20140519 20140603 20140606 20140609 20140612 14299