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D-0870-2023 Class III Terminated

Recalled by HF Acquisition Co LLC — Mukilteo, WA

FDA drug recall D-0870-2023 was initiated by HF Acquisition Co LLC on Jun 6, 2023 and is designated Class III. Reason for recall: Labeling: Label Mix-up The recall status is terminated (terminated Feb 27, 2024). Affected quantity: 9 boxes of 25 vials.

Recall Details

Product Type: Drugs
Report Date: Jun 14, 2023
Initiation Date: Jun 6, 2023
Termination Date: Feb 27, 2024
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 9 boxes of 25 vials

Product Description

GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo, WA 98275, NDC 51662-1487-3

Reason for Recall

Labeling: Label Mix-up

Distribution Pattern

Distributed in TX, AZ and CA only

Code Information

Lot #: 2205095.1, Exp. Date 7/31/2024

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0870-2023
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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