TENSIVE CONDUCTIVE ADHESIVE GELRecalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

1 other recall cover devices cleared under the same FDA submission (K852956); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Feb 7, 2024Class IIOpen, Classified

   Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall related to their Tensive Conductive Adhesive Gel, Ref. 22-60 Lot Number A0623009. They have received five complaints. These customers reported that the gel is too thick, is discolored (darker than usual), and in one instance, patients reported irritation after procedures using the gel.

   Z-1305-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

2. Jan 22, 2024Class IIOpen, Classified

   Five complaints were received related to viscosity of Tensive Conductive Adhesive Gel Ref 22-60.

   Z-1204-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K852956. One submission often covers many models, so check the product and lot details in each record.

• Z-1306-2024 · Feb 7, 2024 · Open, Classified
  natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252