CLASS II Food recall · Reported 12 May 2021 · FDA Enforcement Report
Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap recalled
Natrol is recalling Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap, distributed in 36 states. The recall was initiated on 8 Apr 2021 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0479-2021
- FDA event ID
- 87704
- Recalling firm
- Natrol, Chatsworth, CA
- Brand
- Natrol Melatonin
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 8 Apr 2021
- FDA classified
- 6 May 2021
- Reported
- 12 May 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Other
Timeline
| 8 Apr 2021 | Recall initiated by company | |
| 6 May 2021 | Classified by FDA | +28 days |
| 12 May 2021 | Published 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
One lot of ALA 300 mg Cap-50 were labeled at Melatonin 3 mg Tab-60.
Product as listed by the FDA
Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap. Fall asleep faster, Stay asleep longer, 100$ Drug Free 1 Tablet 20 minutes before bedtime. Manufactured by Natrol LLC. Chatsworth, CA 91311 USA
Where it was distributed
AL, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WI, WV and Ukraine, Serbia, Italy, Trinidad, Croatia
AlabamaArizonaCaliforniaColoradoDelawareFloridaGeorgiaIowaIllinoisIndianaKentuckyLouisianaMassachusettsMarylandMaineMichiganMinnesotaMissouriMississippiNorth Carolina
Questions about this recall
Is Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap recalled?
Yes. Natrol recalled Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap on 8 Apr 2021. The recall is Class II and its status is Terminated. Recall number F-0479-2021.
Why was it recalled?
One lot of ALA 300 mg Cap-50 were labeled at Melatonin 3 mg Tab-60.
Which lots are affected?
Lot 2084395, Expiration DEC31 23
Where was it sold?
AL, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WI, WV and Ukraine, Serbia, Italy, Trinidad, Croatia
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
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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