Bio-Detek, Inc.: Medical Device Recall in 2019 - (Recall #: Z-1945-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)

Product Classification:

Class II

Date Initiated: May 28, 2019

Date Posted: July 10, 2019

Recall Number: Z-1945-2019

Event ID: 83040

Reason for Recall:

Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing therapy.

Status: Terminated

Product Quantity: 1789

Code Information:

Lots 1719, 1719A, and 1819

Distribution Pattern:

Distributed to accounts in AZ, CA, CO, CT, FL, LA, MN, NV, OH, PA, TN, UT, and WY. International distribution to Canada, Germany, France, and Italy.

Voluntary or Mandated:

Voluntary: Firm initiated