---
title: "GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisit... — FDA record D-0870-2023 | Is It on Recall"
description: "Labeling: Label Mix-up"
url: https://isitonrecall.com/recall/fda-drug-d-0870-2023-glycopyrrolate-injection-usp-0-2mg-ml-1ml-vial-manufactured-by-hf-acquisition-co-llc-mukilteo-wa-982/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo, WA 98275, NDC 516... — FDA record D-0870-2023

Reported terminated

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 Jun 6, 2023. 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**: GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo, WA 98275, NDC 51662-1487-3
- **Reason**: Labeling: Label Mix-up
- **Classification**: Class III
- **Recalling firm**: HF Acquisition Co LLC
- **Quantity**: 9 boxes of 25 vials
- **Agency-reported status**: Terminated
- **Source record identifier**: D-0870-2023

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0870-2023%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 | Lot #: 2205095.1, Exp. Date 7/31/2024 |

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

## Distribution

Distributed in TX, AZ and CA only

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/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Jun 14, 2023
- **Recall initiation date**: Jun 6, 2023
- **Center classification date**: Jun 8, 2023
- **Termination date**: Feb 27, 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/drug/enforcement.json?search=recall_number%3A%22D-0870-2023%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [HF Acquisition Co LLC records](https://isitonrecall.com/brand/hf-acquisition-co-llc/)