CLASS II ONGOING Drug recall · Reported 24 Jan 2024 · FDA Enforcement Report

Good Neighbor Pharmacy, Dye Free recalled by Pharma Nobis

Pharma Nobis is recalling Good Neighbor Pharmacy, Dye Free, Sugar Free Magnesium Citrate Saline Laxative, Oral, distributed nationwide in the US. The recall was initiated on 21 Dec 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots A80673, A80742; Exp 10/31/2025
NDC46122-741
Quantity recalled24,684 Bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0227-2024
FDA event ID
93682
Recalling firm
Pharma Nobis, Texarkana, TX
Manufacturer
AMERISOURCE BERGEN
Classification
Class II
Status
Ongoing
Recall initiated
21 Dec 2023
FDA classified
12 Jan 2024
Reported
24 Jan 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Sterility

Timeline

21 Dec 2023Recall initiated by company
12 Jan 2024Classified by FDA+22 days
24 Jan 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Good Neighbor Pharmacy, DYE FREE, SUGAR FREE Magnesium Citrate Saline Laxative, Oral Solution, Cherry Flavor 10 fl. oz, Distributed by AmerisourceBergen, 1 West First Ave, Conshochoken, PA 19428, NDC 46122-741-38

Where it was distributed

Nationwide.

Nationwide

Questions about this recall

Why was it recalled?

MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.

Which lots are affected?

Lots A80673, A80742; Exp 10/31/2025

Where was it sold?

Nationwide.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 93682

This product is part of a recall event; the main page for the event is Freskaro refresh & revitalize Magnesium Citrate Saline recalled.

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