---
title: "Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a b... — FDA record Z-1185-2024 | Is It on Recall"
description: "This IVD is colorless. A customer complaint was received noting it appeared pink. A review of inventory confirmed additional stock appeared pink."
url: https://isitonrecall.com/recall/fda-device-z-1185-2024-schiff-reagent-hotchkiss-mcmanus-packaged-in-an-amber-glass-bottle-with-a-black-polypropylene-cap/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap. — FDA record Z-1185-2024

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 26, 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**: Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.
- **Reason**: This IVD is colorless. A customer complaint was received noting it appeared pink. A review of inventory confirmed additional stock appeared pink.
- **Classification**: Class II
- **Recalling firm**: EMD Millipore Corporation
- **Quantity**: 106 Units (25 US, 81 OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1185-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1185-2024%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 | Part number: 6073-71, 500mL; Lot Numbers (Expiration Date): 3094 (2025-08-04), 3096 (2025-06-28); |

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

## Distribution

Domestic: AL, IL, MA, MN, NJ, PA, TX, VA. Foreign: Canada.

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

- [Alabama](https://isitonrecall.com/state/alabama/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Mar 6, 2024
- **Recall initiation date**: Jan 26, 2024
- **Center classification date**: Feb 23, 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-1185-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [EMD Millipore Corporation records](https://isitonrecall.com/brand/emd-millipore-corporation/)