BD Microtainer Quikheel Lancet Recalled for Failure to Retract
Becton Dickinson is recalling BD Microtainer Quikheel Lancets because they may not retract after use, creating a risk of exposure to used sharps.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (exposure to used sharps) where no specific injuries or illnesses have been reported in the source text, fitting the criteria for a High severity score.
Plain-English summary
Becton Dickinson & Company is recalling BD Microtainer Quikheel Lancets (REF 368101, Lot #3116007). The device is used to perform heel sticks for collecting skin puncture blood. The recall involves 39,800 units distributed in the United States and 18,400 units in Canada.
The recall is being conducted because the lancet may fail to retract after activation. This defect creates a potential for exposure to a used sharp. The product was distributed in the states of Connecticut, Kentucky, Illinois, New York, Pennsylvania, Texas, and Virginia, as well as in Canada.
Consumers and healthcare providers should stop using the affected lancets and contact Becton Dickinson & Company for further instructions or a replacement.
The recalled product
- 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.
- Manufacturer
- Becton Dickinson & Company
Distribution
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