Recall Z-1636-2016— Hummingbird Med
Class I · Terminated
Class I FDA medical device recall by Hummingbird Med, initiated 2015-10-01, terminated 2017-01-26. FDA's recall record names no specific 510(k) clearance for this event. Product: ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is used for blood transfer and collection from Peripheral Arterial Line Catheters.. Reason: Hummingbird Med Devices, Inc. is recalling ABG-HM-1 Hummi Micro Draw Blood Transfer because the connection between the "Hummi" Y connector and the yellow cannula hub may not be sufficiently secure enough and could separate while in use..
- Recalling firm
- Hummingbird Med
- Classification
- Class I
- Status
- Terminated
- Initiated
- 2015-10-01
- Terminated
- 2017-01-26
- Firm location
- Lake Forest, CA, United States
Product description
ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is used for blood transfer and collection from Peripheral Arterial Line Catheters.
Reason for recall
Hummingbird Med Devices, Inc. is recalling ABG-HM-1 Hummi Micro Draw Blood Transfer because the connection between the "Hummi" Y connector and the yellow cannula hub may not be sufficiently secure enough and could separate while in use.
Data sourced from openFDA. This site is unofficial and independent of the FDA.