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

Lot, batch or date codesLot Nos.: 1147550, exp. Sept 2017; 1174782, exp. JUL 2018; 1176755, exp. JUL2018
Quantity recalled161507 units

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
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
E-Mail
Reason category
Mold
Product category
Vitamins

Timeline

6 Jun 2016Recall initiated by company
2 Sep 2016Classified by FDA+88 days
14 Sep 2016Published 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

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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