CLASS II Food recall · Reported 19 Jul 2017 · FDA Enforcement Report
Source Naturals Renewal Antioxidant Tablet: Sample Pack recalled
Threshold Enterprises is recalling Source Naturals Renewal Antioxidant Tablet: Sample Pack, & per, distributed nationwide in the US. The recall was initiated on 11 Sep 2015 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-2383-2017
- FDA event ID
- 77531
- Recalling firm
- Threshold Enterprises, Scotts Valley, CA
- Brand
- Source Naturals
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 11 Sep 2015
- FDA classified
- 10 Jul 2017
- Reported
- 19 Jul 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Allergens
- Product category
- Dietary Supplements
Timeline
| 11 Sep 2015 | Recall initiated by company | |
| 10 Jul 2017 | Classified by FDA | +668 days |
| 19 Jul 2017 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Dietary supplements contain low levels of undeclared boron
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count Bottle - Product SN1752; 10 Count Sample Packs - Product SN5024. Manufactured for Source Naturals, Santa Cruz, CA
Where it was distributed
Nationwide only.
Questions about this recall
Is Source Naturals Renewal Antioxidant Tablet: Sample Pack, & per recalled?
Yes. Threshold Enterprises recalled Source Naturals Renewal Antioxidant Tablet: Sample Pack, & per on 11 Sep 2015. The recall is Class II and its status is Terminated. Recall number F-2383-2017.
Why was it recalled?
Dietary supplements contain low levels of undeclared boron
Which lots are affected?
30 Count bottles: Lot No. QTY Exp. FG-13852 76 12/15 FG-14726 148 12/15 FG-19274 148 03/16 FG-24304 148 03/16 FG-30636 100 03/16 FG-37569 9 03/16 FG-39616 172 07/17 FG-47423 64 07/17 FG-50614 70 07/17 FG-65266 60 07/17 FG-65266 60 07/17 FG-59256 144 09/18 60 count bottles: Lot No. QTY Exp. FG-13853 338 12/15 FG-14725 468 12/15 FG-19145 290 03/16 FG-23361 206 03/16 FG-23362 396 03/16 FG-34451 98 03/16 FG-38199 38 03/16 FG-39615 424 07/17 FG-50331 122 07/17 FG-53623 144 07/17 FG-59257 362 09/18 FG-65017 206 09/18 120 count bottles: LOT QTY EXP FG-13854 134 12/15 FG-14556 141 12/15 FG-15360 213 12/15 FG-19882 302 03/16 FG-23397 350 03/16 FG-29559 160 03/16 FG-32109 215 03/16 FG-32109 215 03/16 FG-37240 60 03/16 FG-38639 42 03/16 FG-39812 444 07/17 FG-45840 266 07/17 FG-51761 200 07/17 FG-59258 482 09/18 FG-64221 218 09/18 FG-65613 395 09/18; 10 count sample packs; Lot No. QTY Exp. FG-13855 41 12/15 FG-30136 108 03/16 FG-34834 95 03/16 FG-39626 200 07/17 FG-43530 277 07/17 FG-51677 150 07/17 FG-59259 362 09/18
Where was it sold?
Nationwide only.
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.
More recalls from Threshold Enterprises
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|---|---|---|---|---|---|
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