Steris Corporation: Medical Device Recall in 2012 - (Recall #: Z-2284-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

QKC1692E The QKC1692E Quick Connect device connects endoscopes to the sterilization tray for C1220E liquid chemical sterilization processor.

Product Classification:

Class II

Date Initiated: August 10, 2012

Date Posted: September 5, 2012

Recall Number: Z-2284-2012

Event ID: 62776

Reason for Recall:

STERIS has been actively seeking devices for quick connect revalidation projects. STERIS was unable to obtain two (2) of the needed devices; these two devices represent the design of seven (7) models in one quick connect. Due to the unavailability of these two validation devices, STERIS will remove 7 models from the labeling of QKC1692E and will re-label all QKC1692Es in the field..

Status: Terminated

Product Quantity: 64 units

Code Information:

Lot numbers: 1879717, 1943786, 2054914, 2143717, 2177723, 2342319, 2730752, 2922565, 3094190

Distribution Pattern:

Nationwide distribution: USA including states of: AR, AK, CA, CO, DE, FL, IL, MA, MD, NC, NE, NH, NY, OH, PA, SD, TN, TX, WI, and WV.

Voluntary or Mandated:

Voluntary: Firm initiated