CLASS II Drug recall · Reported 4 Nov 2020 · FDA Enforcement Report

N-a-c (N-Acetyl-L-Cysteine, 500 mg recalled by Jarrow Formulas

Jarrow Formulas is recalling N-a-c (N-Acetyl-L-Cysteine, 500 mg, distributed nationwide in the US. The recall was initiated on 9 Oct 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 65323G20; Expiration: 7/22
Quantity recalled533 units

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-0302-2021
FDA event ID
86617
Recalling firm
Jarrow Formulas, Los Angeles, CA
Classification
Class II
Status
Terminated
Recall initiated
9 Oct 2020
FDA classified
29 Oct 2020
Reported
4 Nov 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Labeling Errors

Timeline

9 Oct 2020Recall initiated by company
29 Oct 2020Classified by FDA+20 days
4 Nov 2020Published in enforcement report+6 days

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

Reason for recall

Mislabeling of SUS (N-A-C Sustain 600 mg 100 tab) with N-A-C N-Acetyl-L-Cysteine 500 mg, 100 cap.

Product as listed by the FDA

N-A-C (N-Acetyl-L-Cysteine, 500 mg, 100 capsules; Veggie Caps, white HDPE bottle with RED label Product # 107002 UPC: 790011070023

Where it was distributed

Nationwide.

Nationwide

Questions about this recall

Is N-a-c (N-Acetyl-L-Cysteine, 500 mg recalled?

Yes. Jarrow Formulas recalled N-a-c (N-Acetyl-L-Cysteine, 500 mg on 9 Oct 2020. The recall is Class II and its status is Terminated. Recall number D-0302-2021.

Why was it recalled?

Mislabeling of SUS (N-A-C Sustain 600 mg 100 tab) with N-A-C N-Acetyl-L-Cysteine 500 mg, 100 cap.

Which lots are affected?

Lot 65323G20; Expiration: 7/22

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

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