Recall Z-2192-2013— Becton Dickinson & Company
Class II · Terminated
Class II FDA medical device recall by Becton Dickinson & Company, initiated 2013-07-10, terminated 2014-03-19. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lakes, NJ 07417 USA Made in USA. Used to perform heel sticks for the purpose of collecting skin puncture blood.. Reason: The Lancet will not retract after activation thus creating a potential for exposure to a used sharp..
- Recalling firm
- Becton Dickinson & Company
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-07-10
- Terminated
- 2014-03-19
- Firm location
- Franklin Lakes, NJ, United States
Product description
BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lakes, NJ 07417 USA Made in USA. Used to perform heel sticks for the purpose of collecting skin puncture blood.
Reason for recall
The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
Data sourced from openFDA. This site is unofficial and independent of the FDA.