FDAFDA · Food and drugs·Recall number Z-2192-2013
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.
Published September 18, 2013 · Recall initiated: July 10, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Becton Dickinson & Company
- Distributor
- Distributed in the states of CT, KY, IL, NY, PA, TX, and VA and the country of Canada.
- Lot
- REF # 368101 Lot #3116007 Class I Exempt Device listing Number E158602
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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