Becton Dickinson & Company: Medical Device Recall in 2013 - (Recall #: Z-2192-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: July 10, 2013

Date Posted: September 18, 2013

Recall Number: Z-2192-2013

Event ID: 66031

Reason for Recall:

The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.

Status: Terminated

Product Quantity: US - 39,800 units ; Canada - 18,400 units

Code Information:

REF # 368101 Lot #3116007 Class I Exempt Device listing Number E158602

Distribution Pattern:

Distributed in the states of CT, KY, IL, NY, PA, TX, and VA and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated