---
title: "Graphic Controls Acquisition Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Graphic Controls Acquisition Corporation recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/graphic-controls-acquisition-corporation/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Graphic Controls Acquisition Corporation recall records

**0** reported ongoing

6 records in this archive. Latest source date Mar 15, 2022.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

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/).

## Records and reported status

Mar 15, 2022 FDA device enforcement

### [CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US](https://isitonrecall.com/recall/fda-device-z-0935-2022-claravue-pre-wired-electrode-ip-set-n3-pediatric-us-model-32028776-50401-us/)

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c...

Class II Reported terminated

Distribution: US Nationwide distribution in the States of AR, CA, CO, FL, IN, KS, MA, MN, NY, OK, VT.

[Official source for CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0935-2022%22)

Mar 15, 2022 FDA device enforcement

### [CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600 US](https://isitonrecall.com/recall/fda-device-z-0936-2022-claravue-pre-wired-electrode-ip-set-m3-rt-adult-us-model-32028777-50600-us/)

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c...

Class II Reported terminated

Distribution: US Nationwide distribution in the States of AR, CA, CO, FL, IN, KS, MA, MN, NY, OK, VT.

[Official source for CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600 US](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0936-2022%22)

Mar 15, 2022 FDA device enforcement

### [CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778 50601-US](https://isitonrecall.com/recall/fda-device-z-0937-2022-claravue-pre-wired-electrode-ip-set-m5-rt-adult-us-model-32028778-50601-us/)

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c...

Class II Reported terminated

Distribution: US Nationwide distribution in the States of AR, CA, CO, FL, IN, KS, MA, MN, NY, OK, VT.

[Official source for CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778 50601-US](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0937-2022%22)

Mar 15, 2022 FDA device enforcement

### [CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779 50602-US](https://isitonrecall.com/recall/fda-device-z-0938-2022-claravue-pre-wired-electrode-ip-set-12-rt-adult-us-model-32028779-50602-us/)

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c...

Class II Reported terminated

Distribution: US Nationwide distribution in the States of AR, CA, CO, FL, IN, KS, MA, MN, NY, OK, VT.

[Official source for CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779 50602-US](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0938-2022%22)

Mar 15, 2022 FDA device enforcement

### [CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780 50603-US](https://isitonrecall.com/recall/fda-device-z-0939-2022-claravue-pre-wired-electrode-ip-set-6v-rt-adult-us-model-32028780-50603-us/)

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c...

Class II Reported terminated

Distribution: US Nationwide distribution in the States of AR, CA, CO, FL, IN, KS, MA, MN, NY, OK, VT.

[Official source for CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780 50603-US](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0939-2022%22)

Mar 15, 2022 FDA device enforcement

### [CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US](https://isitonrecall.com/recall/fda-device-z-0940-2022-claravue-pre-wired-electrode-ip-set-5v-rt-adult-model-32028781-50604-us/)

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c...

Class II Reported terminated

Distribution: US Nationwide distribution in the States of AR, CA, CO, FL, IN, KS, MA, MN, NY, OK, VT.

[Official source for CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0940-2022%22)

## Reasons in these listed records

- Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c. when used with a d...

These examples come from this result page and are not a ranking of every recall reason.

## Checking Graphic Controls Acquisition Corporation

### Is there a recall on graphic controls acquisition corporation right now?

This archive contains 6 records, including 0 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search Graphic Controls Acquisition Corporation](https://isitonrecall.com/check/?q=Graphic%20Controls%20Acquisition%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
