FDA Device recall Z-1908-2016
ABG-HM-1 Hummi Micro Draw Blood Transfer Device
- FDA Device
- Class I
- terminated
- Published 2016-07-13
On 2016-07-13 the FDA classified a Class I recall of ABG-HM-1 Hummi Micro Draw Blood Transfer Device by Hummingbird Med, citing hummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of insertion difficulties.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1908-2016 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-03-11 |
| Published | 2016-07-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Hummingbird Med |
| Distribution | CA |
Product
ABG-HM-1 Hummi Micro Draw Blood Transfer Device; Used for blood transfer and collection from peripheral arterial line catheters.
Reason
Hummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of insertion difficulties.
Identifiers
| code_info | Lot Numbers: 20140510 20140513 20140516 20140519 20140603 20140606 20140609 20140612 14299 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1908-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.