CLASS III Food recall · Reported 28 Jul 2021 · FDA Enforcement Report
Kroger Vitamin D, Green HDPE packaging recalled by Bountiful Trading
Bountiful Trading is recalling Kroger Vitamin D, Green HDPE packaging, distributed in Arizona, Colorado, Indiana, Tennessee, Wisconsin. The recall was initiated on 9 Jul 2021 and the FDA has classified it as Class III.
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-0789-2021
- FDA event ID
- 88263
- Recalling firm
- Bountiful Trading, New York, NY
- Brand
- Kroger
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 9 Jul 2021
- FDA classified
- 20 Jul 2021
- Reported
- 28 Jul 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Packaging Defects
- Product category
- Vitamins
Timeline
| 9 Jul 2021 | Recall initiated by company | |
| 20 Jul 2021 | Classified by FDA | +11 days |
| 28 Jul 2021 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Vitamin D dietary supplement may contain Coq10
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging
Where it was distributed
IN, TN, WI, CO, AZ
ArizonaColoradoIndianaTennesseeWisconsin
Stores named: Kroger
Questions about this recall
Why was it recalled?
Vitamin D dietary supplement may contain Coq10
Which lots are affected?
Prod # 19937, Lot # 508981-02, Exp 02/24 041260351211
Where was it sold?
IN, TN, WI, CO, AZ
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
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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