Nature Made Vitamin D3 Recall: Yeast/Mold Exceeding Specs
Pharmavite recalls specific Nature Made Vitamin D3 tablets due to yeast and mold levels exceeding specifications. Check your lot number.
Use caution until it’s fixed
Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Contact the company
What happened, in plain English
Pharmavite is recalling specific lots of Nature Made Vitamin D3 1000IU tablets because they may exceed safety specifications for yeast and mold. The affected product is a 125-count bottle with UPC 0-31604-02793-3. This recall covers approximately 23,865 units distributed nationwide. Read more at govinfonow.com/recall/24113-nature-made-vitamin-d3-recall-yeast-mold-exceeding-specs.
Source Summary by GovInfoNow · govinfonow.com/recall/24113-nature-made-vitamin-d3-recall-yeast-mold-exceeding-specs · Updated October 9, 2026 · FDA enforcement record: FDA #F-2077-2016
Cite this page
“Nature Made Vitamin D3 Recall: Yeast/Mold Exceeding Specs.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/24113-nature-made-vitamin-d3-recall-yeast-mold-exceeding-specs. Based on FDA recall #F-2077-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2077-2016%22&limit=1).
Why it’s dangerous
The recalled tablets may contain levels of yeast and mold that exceed established specifications. While the record does not specify immediate injury symptoms, consuming supplements with excessive microbial growth can pose health risks, particularly for sensitive individuals.
Who’s affected
Consumers who purchased Nature Made Vitamin D3 1000IU tablets in 125-count bottles between unspecified dates prior to June 2016. Individuals with compromised immune systems or mold allergies may be at higher risk from the potential yeast/mold contamination.
How to tell if you have this one
Check your bottle for the UPC code 0-31604-02793-3 and Lot Number 1147978. The product is Nature Made Vitamin D3 1000IU in a 125-count package with an expiration date of SEPT 2017.
- Brand
Nature Made- Product
Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3- Category
Food
All 14 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-2065-2016 | Nature Made(R) adult gummies Multi, 90 count, UPC 0-31604-02841-1; Lot No. 1196066, exp. AUG 2017 | 2076 units |
| F-2066-2016 | Nature Made(R) adult gummies Multi, 150 count, UPC 0-31604-04172-4; Lot Nos.: 1196071, AUG 2017; exp. 1205052, exp. OCT 2017 | 6132 units |
| F-2067-2016 | Nature Made(R) Multi + Omega-3, 150 count, UPC 0-31604-04173-1; Lot No. 1173600, exp. JAN 2017 | 10836 units |
| F-2068-2016 | Nature Made(R) adult gummies Multi for Her plus Omega-3, 100 count, UPC 0-31604-04236-3; Lot No. 1196048, exp. AUG 2017 | 6792 units |
| F-2069-2016 | Nature Made(R) adult gummies Multi for Her plus Omega-3, 150 count, UPC 0-31604-04275-2; Lot No. 1196050, exp. AUG 2017 | 15504 units |
| F-2070-2016 | Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 140 count, UPC 0-31604-02727-8; Lot No. 1173779, exp. JUL 2017 | 78642 units |
| F-2071-2016 | Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 460 count, UPC 0-31604-02728-5; Lot Nos.: 1170987, exp. JUL 2017; 1204735, exp. MAR 2018 | 70,540 units |
| F-2072-2016 | Nature Made (R) Super B-Complex, KEY B VITAMINS + VITAMIN C, 360 count, UPC 0-31604-02729-2; Lot Nos.: 1173146, exp. JUL 2017; 1204001, exp. MAR 2018 | 134,028 units |
| F-2073-2016 | Nature Made(R) adult gummies Hair.Skin.Nails, 90 count, UPC 0-31604-04016-1; Lot No. 1198437, exp. SEPT 2017 | 14604 units |
| F-2074-2016 | Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC 0-31604-04132-8-1; Lot No. 1198438, exp. SEPT 2017 | 11136 units |
| F-2075-2016 | Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2; Lot Nos.: 1147550, exp. Sept 2017; 1174782, exp. JUL 2018; 1176755, exp. JUL2018 | 161507 units |
| F-2076-2016 | Nature Made(R) D3 1000IU, 300 count, UPC 0-31604-02683-7; Lot Nos.: 1140172, exp. SEPT 2017; 1175637, exp. JUL 2018; 1176756, exp. JUL 2018 | 91329 units |
| F-2077-2016 | Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3; Lot No. 1147978, exp. SEPT 2017 | 23865 units |
| F-2078-2016 | Nature Made(R) D3 1000IU, 350 count, UPC 0-31604-04070-3; Lot No. 1177557, exp. SEPT 2017 | 30480 units |
What to do — step by step
Check your bottle
Verify if your bottle has UPC 0-31604-02793-3 and Lot No. 1147978.
Contact Pharmavite
The record does not specify a remedy or return process, so contact the manufacturer for instructions.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-2077-2016 (June 6, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2077-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.