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

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

# Remel Inc recall records

**15** reported ongoing

25 records in this archive. Latest source date Jun 3, 2026.

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

Jun 3, 2026 FDA device enforcement

### [GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460](https://isitonrecall.com/recall/fda-device-z-2623-2026-gc-agar-base-150mm-10-pk-r04030-gc-agar-base-100mm-10-pk-r01460/)

Reduced or no recovery of some strains of Neisseria gonorrhoeae.

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Singapore, and the United Kingdom.

[Official source for GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2623-2026%22)

Mar 24, 2026 FDA device enforcement

### [Yeastone Broth, 11ML, 10/BOX YY3462](https://isitonrecall.com/recall/fda-device-z-1806-2026-yeastone-broth-11ml-10-box-yy3462/)

Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Vietnam, France, Argentina, Qatar, New Zealand, Uruguay, Turkey, Netherlands, Singapore.

[Official source for Yeastone Broth, 11ML, 10/BOX YY3462](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1806-2026%22)

Feb 5, 2026 FDA device enforcement

### [Campy CVA Medium 100/PK, R01272](https://isitonrecall.com/recall/fda-device-z-1474-2026-campy-cva-medium-100-pk-r01272/)

Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.

Class II Reported ongoing

Distribution: US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.

[Official source for Campy CVA Medium 100/PK, R01272](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1474-2026%22)

Nov 12, 2025 FDA device enforcement

### [1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450](https://isitonrecall.com/recall/fda-device-z-0585-2026-1-camhb-w-lhb-manual-11ml-10-box-ycp112-10-2-brucella-broth-11ml-10-box-yt3450/)

Products may contain contamination, which may result in a darker or brown media color.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of AK, CA, FL, GA, IA, IL, IN, LA, MA, MD, ME, MI, MN, NE, NY, OH, OK, PA, RI, SD, TN, VA, WA, WI and the countries of Brazi...

[Official source for 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0585-2026%22)

Jul 11, 2025 FDA device enforcement

### [Blood Agar,5% Sheep Blood 100/PK, Product Number R01202](https://isitonrecall.com/recall/fda-device-z-2223-2025-blood-agar-5-sheep-blood-100-pk-product-number-r01202/)

The products may contain surface and subsurface contamination of Listeria monocytogenes.

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Blood Agar,5% Sheep Blood 100/PK, Product Number R01202](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2223-2025%22)

Jul 11, 2025 FDA device enforcement

### [Strep Selective II Agar, Product Number R01859](https://isitonrecall.com/recall/fda-device-z-2224-2025-strep-selective-ii-agar-product-number-r01859/)

The products may contain surface and subsurface contamination of Listeria monocytogenes.

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Strep Selective II Agar, Product Number R01859](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2224-2025%22)

Jul 11, 2025 FDA device enforcement

### [Blood/EMB, Levine 100/PK, Product Number R02041](https://isitonrecall.com/recall/fda-device-z-2225-2025-blood-emb-levine-100-pk-product-number-r02041/)

The products may contain surface and subsurface contamination of Listeria monocytogenes.

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Blood/EMB, Levine 100/PK, Product Number R02041](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2225-2025%22)

Jul 11, 2025 FDA device enforcement

### [Blood/MacConkey Biplate 100/PK, Product Number R02049](https://isitonrecall.com/recall/fda-device-z-2226-2025-blood-macconkey-biplate-100-pk-product-number-r02049/)

The products may contain surface and subsurface contamination of Listeria monocytogenes.

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for Blood/MacConkey Biplate 100/PK, Product Number R02049](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2226-2025%22)

May 1, 2025 FDA device enforcement

### [Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic device](https://isitonrecall.com/recall/fda-device-z-1947-2025-thermo-scientific-sensititre-cation-adjusted-autoread-mueller-hinton-broth-w-tes-w-lysed-horse-blood/)

Product may have an off color affecting perfomance

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the states of AL, GA, KY, VA and the countries of Canada, UK.

[Official source for Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1947-2025%22)

Feb 13, 2025 FDA device enforcement

### [remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use](https://isitonrecall.com/recall/fda-device-z-1200-2025-remel-blood-agar-macconkey-agar-biplate-ref-r02049-qty-100-for-invitro-diagnostic-use/)

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1200-2025%22)

Feb 13, 2025 FDA device enforcement

### [remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use](https://isitonrecall.com/recall/fda-device-z-1201-2025-remel-blood-agar-emb-agar-biplate-ref-r02041-qty-100-for-invitro-diagnostic-use/)

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

Class II Reported ongoing

Distribution: US Nationwide distribution.

[Official source for remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1201-2025%22)

Feb 12, 2025 FDA device enforcement

### [Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ system YV4000-VZ](https://isitonrecall.com/recall/fda-device-z-1395-2025-zebra-thermal-barcode-printer-gx430t-model-no-ysw-1000-or-ysw-2000-may-have-been-sold-as-an-optional/)

Power supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.

Class II Reported ongoing

Distribution: Domestic distribution to AL, AZ, CA, FL, GA, IN, KS, KY, MD, MI, NE, NY, OH, PA, TN, TX, WI. International distribution to Canada and the Bahamas.

[Official source for Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an op...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1395-2025%22)

Sep 20, 2024 FDA device enforcement

### [remel BactiDrop Acridine Orange, REF 21502, 50 per package.](https://isitonrecall.com/recall/fda-device-z-0266-2025-remel-bactidrop-acridine-orange-ref-21502-50-per-package/)

A color change of the solution within the dropper can occur from orange-yellow to light yellow resulting in out-of-specification fluorescent stain results.

Class II Reported ongoing

Distribution: Distribution was made to IL, IN, MN, NE, SD, TX, VA, and WA. There was government distribution but no military distribution. Foreign distribution was made to the United Kingdom.

[Official source for remel BactiDrop Acridine Orange, REF 21502, 50 per package.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0266-2025%22)

Aug 14, 2023 FDA device enforcement

### [remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clinical specimens containing mixed bacterial flora](https://isitonrecall.com/recall/fda-device-z-2531-2023-remel-todd-hewitt-w-cna-lim-broth-ref-r064810-used-to-isolate-group-b-streptococci-form-clinical-spe/)

On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target organism during customer QC testing or use with patient samples

Class II Reported ongoing

Distribution: US Nationwide Distribution

[Official source for remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clin...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2531-2023%22)

May 31, 2023 FDA device enforcement

### [Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In Vitro Diagnostic Use.](https://isitonrecall.com/recall/fda-device-z-2038-2023-remel-haemophilus-test-medium-agar-150mm-10-pk-ref-r04033-and-remel-haemophilus-test-medium-agar-100/)

The test medium may not perform as intended.

Class II Reported ongoing

Distribution: Distribution was made nationwide, including Puerto Rico. There was no foreign or military distribution.

[Official source for Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Mediu...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2038-2023%22)

Oct 20, 2022 FDA device enforcement

### [Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST](https://isitonrecall.com/recall/fda-device-z-0327-2023-thermo-scientific-sensititre-plate-gn4f-gram-negative-ivd-ast/)

An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripen...

Class I Reported terminated

Distribution: US Nationwide Distribution

[Official source for Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0327-2023%22)

Oct 20, 2022 FDA device enforcement

### [Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST](https://isitonrecall.com/recall/fda-device-z-0328-2023-thermo-scientific-sensititre-gn6f-gram-negative-ivd-ast/)

An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripen...

Class I Reported terminated

Distribution: US Nationwide Distribution

[Official source for Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0328-2023%22)

Oct 20, 2022 FDA device enforcement

### [Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST](https://isitonrecall.com/recall/fda-device-z-0329-2023-thermo-scientific-sensititre-gn7f-gram-negative-ivd-ast/)

An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripen...

Class I Reported terminated

Distribution: US Nationwide Distribution

[Official source for Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0329-2023%22)

Oct 20, 2022 FDA device enforcement

### [Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST](https://isitonrecall.com/recall/fda-device-z-0330-2023-thermo-scientific-sensititre-hpb1-gram-negative-ivd-ast/)

An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripen...

Class I Reported terminated

Distribution: US Nationwide Distribution

[Official source for Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0330-2023%22)

Oct 20, 2022 FDA device enforcement

### [Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST](https://isitonrecall.com/recall/fda-device-z-0331-2023-thermo-scientific-sensititre-cmc5vgnf-gram-negative-ivd-ast/)

An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripen...

Class I Reported terminated

Distribution: US Nationwide Distribution

[Official source for Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0331-2023%22)

## Reasons in these listed records

- Reduced or no recovery of some strains of Neisseria gonorrhoeae.
- Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.
- Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
- Products may contain contamination, which may result in a darker or brown media color.

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

## Checking Remel Inc

### Is there a recall on remel inc right now?

This archive contains 25 records, including 15 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 Remel Inc](https://isitonrecall.com/check/?q=Remel%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
