Recall Z-0572-2015— Becton Dickinson & Company
Class II · Terminated
Class II FDA medical device recall by Becton Dickinson & Company, initiated 2014-10-09, terminated 2015-04-24. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Insyte Autoguard Catheter An active safety engineered peripheral IV catheter with a retracting needle to reduce accidental needle stick injuries. The safety feature (needle retraction) of this device is activated when the clinician depresses the button located on the superior surface of the grip. This product is used to provide access to the intravascular system for administration of fluids, medication, blood and blood products and for the withdrawal of the blood samples.. Reason: BD Insyte Autoguard may have potential damage along the body of the catheter..
- Recalling firm
- Becton Dickinson & Company
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-10-09
- Terminated
- 2015-04-24
- Firm location
- Franklin Lakes, NJ, United States
Product description
BD Insyte Autoguard Catheter An active safety engineered peripheral IV catheter with a retracting needle to reduce accidental needle stick injuries. The safety feature (needle retraction) of this device is activated when the clinician depresses the button located on the superior surface of the grip. This product is used to provide access to the intravascular system for administration of fluids, medication, blood and blood products and for the withdrawal of the blood samples.
Reason for recall
BD Insyte Autoguard may have potential damage along the body of the catheter.
Data sourced from openFDA. This site is unofficial and independent of the FDA.