CLASS I Food recall · Reported 29 Sep 2021 · FDA Enforcement Report
Dried Apricot Subkhon with Bone recalled by Golden Natural Products
Golden Natural Products is recalling Dried Apricot Subkhon with Bone, distributed in California, New York, Washington. The recall was initiated on 2 Aug 2021 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-1006-2021
- FDA event ID
- 88380
- Recalling firm
- Golden Natural Products, Brooklyn, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 2 Aug 2021
- FDA classified
- 22 Sep 2021
- Reported
- 29 Sep 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Sulfites
- Product category
- Peaches
Timeline
| 2 Aug 2021 | Recall initiated by company | |
| 22 Sep 2021 | Classified by FDA | +51 days |
| 29 Sep 2021 | Published in enforcement report | +7 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 high levels of undeclared sulfites.
Product as listed by the FDA
Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and Golden Natural Product Inc. brand Dried Apricot Subkhon Jumbo, Net Wt. 16 oz (1 lb) 454 g Manufactured and Packed by: Gardencells LLC, Urgut, Samarkand region Republic of Uzbekistan; Distributed in USA by: GOLDEN NATURAL PRODUCTS INC.
Where it was distributed
NY, CA, WA
Questions about this recall
Why was it recalled?
Product contains high levels of undeclared sulfites.
Which lots are affected?
Lot: GC005 Exp: 2023
Where was it sold?
NY, CA, WA
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.
Other Peaches recalls
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|---|---|---|---|---|---|
| Food | CLASS II | Joy Peach Lassi recalled by Joy Gourmet FoodsJoy Peach | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | Sticker label (for Loose Bulk - yellow peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Moonlight Packing products recalledRecalled | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Sticker label (for Loose Bulk - peppermint peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Sticker label (for Loose Bulk - yellow peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |