CLASS I Food recall · Reported 13 May 2020 · FDA Enforcement Report
Tainy Boctoka Dry Fruits Mix Compot Apple recalled
Royal International Trading is recalling Tainy Boctoka Dry Fruits Mix Compot Apple, distributed in 11 states. The recall was initiated on 22 Apr 2020 and the FDA has classified it as Class I.
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-0937-2020
- FDA event ID
- 85546
- Recalling firm
- Royal International Trading, Brooklyn, NY
- Brand
- Tainy Boctoka
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 22 Apr 2020
- FDA classified
- 7 May 2020
- Reported
- 13 May 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Undeclared Sulfites
- Product category
- Apples
Timeline
| 22 Apr 2020 | Recall initiated by company | |
| 7 May 2020 | Classified by FDA | +15 days |
| 13 May 2020 | 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
Product contains undeclared sulfites.
Product as listed by the FDA
TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE; Assorted dried fruits; NET WT 17.63 oz (500g) clear plastic package
Where it was distributed
MA, CT, NJ, VA, FL, MN, IL, PA, NY, OH, IN
ConnecticutFloridaIllinoisIndianaMassachusettsMinnesotaNew JerseyNew YorkOhioPennsylvaniaVirginia
Questions about this recall
Why was it recalled?
Product contains undeclared sulfites.
Which lots are affected?
Container code 4705932006197
Where was it sold?
MA, CT, NJ, VA, FL, MN, IL, PA, NY, OH, IN
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 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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