---
title: "Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 i... — FDA record Z-1204-2024 | Is It on Recall"
description: "Five complaints were received related to viscosity of Tensive Conductive Adhesive Gel Ref 22-60."
url: https://isitonrecall.com/recall/fda-device-z-1204-2024-tensive-conductive-adhesive-gel-product-ref-22-60-12-1-case-contains-12-inner-boxes-with-50g-tubes-p/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each. — FDA record Z-1204-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 22, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each.
- **Reason**: Five complaints were received related to viscosity of Tensive Conductive Adhesive Gel Ref 22-60.
- **Classification**: Class II
- **Recalling firm**: Parker Laboratories, Inc.
- **Quantity**: 44 cases (6,336 units) (39 cases US, 5 cases OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1204-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1204-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Product Number: 22-60; UDI/DI: (Master)20855683006337, (Inner Box) 10855683006330, (Individual Unit) 00855683006333; Lot A0623009. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US (Domestic): AZ, CA, FL, NC, NJ, NV, NY, PA, WA, WI. OUS (Foreign): Canada, France and Germany.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Washington](https://isitonrecall.com/state/washington/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Mar 6, 2024
- **Recall initiation date**: Jan 22, 2024
- **Center classification date**: Feb 29, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1204-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Parker Laboratories, Inc. records](https://isitonrecall.com/brand/parker-laboratories-inc/)