Abbott Medical: Medical Device Recall in 2019 - (Recall #: Z-0664-2020)

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:

Radiofrequency Grounding Pad, REF RF-DGP-L

Product Classification:

Class II

Date Initiated: October 14, 2019

Date Posted: December 18, 2019

Recall Number: Z-0664-2020

Event ID: 84272

Reason for Recall:

Affected lots were manufactured with the protective release liner in an incorrect orientation. When attempting to remove this disposable release liner, a clear film may be left on the grounding pad which may interfere with patient skin contact and lead to uneven heating.

Status: Terminated

Product Quantity: 8940 devices

Code Information:

UDI: 05415067028914 Batch Numbers: 810319004, 810319005, and 810319021

Distribution Pattern:

nationwide

Voluntary or Mandated:

Voluntary: Firm initiated