CLASS II Food recall · Reported 14 Sep 2016 · FDA Enforcement Report
Nature Made(R) D3 1000IU recalled by Pharmavite
Pharmavite is recalling Nature Made(R) D3 1000IU, distributed nationwide in the US. The recall was initiated on 6 Jun 2016 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-2075-2016
- FDA event ID
- 74400
- Recalling firm
- Pharmavite, Northridge, CA
- Brand
- Nature Made
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Jun 2016
- FDA classified
- 2 Sep 2016
- Reported
- 14 Sep 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Mold
- Product category
- Vitamins
Timeline
| 6 Jun 2016 | Recall initiated by company | |
| 2 Sep 2016 | Classified by FDA | +88 days |
| 14 Sep 2016 | Published 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
Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Product as listed by the FDA
Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2
Where it was distributed
nationwide
Questions about this recall
Is Nature Made(R) D3 1000IU recalled?
Yes. Pharmavite recalled Nature Made(R) D3 1000IU on 6 Jun 2016. The recall is Class II and its status is Terminated. Recall number F-2075-2016.
Why was it recalled?
Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Which lots are affected?
Lot Nos.: 1147550, exp. Sept 2017; 1174782, exp. JUL 2018; 1176755, exp. JUL2018
Where was it sold?
nationwide
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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