Welby Vitamin B12 Adult Gummies recall (July 2025): reason, lots, what to do
Not medical advice. This page reproduces one FDA enforcement report and explains its fields; FDA’s text is quoted as FDA’s. If you have this product and any symptoms, your pharmacist or doctor comes before this page.
What was recalled
Vita Warehouse Corp. (Ronkonkoma, NY) recalled Welby Vitamin B12 Adult Gummies in a recall FDA classified as Class I. FDA’s stated reason: “Contains undeclared peanut”. Started June 11, 2025; posted in the enforcement report July 9, 2025; status Terminated.
Class I means, in FDA’s words, a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. Distribution: “Nationwide”. Quantity: 40,522 bottles plus 582,000 individual gummies. Check your lot →
The FDA record
Everything in this table is copied from FDA’s enforcement report for event 97062, retrieved from openFDA on September 21, 2026; the last row links to the live record so you can confirm it has not changed.
| Recalling firm | Vita Warehouse Corp., Ronkonkoma, NY |
|---|---|
| Product | 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe" Vitamin B12 Extra Strength Gummies 140 count 3. Vita Labs Vitamin B-12 Gummies Bulk 500 count |
| Reason for recall (FDA’s text) | “Contains undeclared peanut” |
| Classification | Class I |
| Status | Terminated |
| Recall type | Voluntary: Firm initiated |
| Recall initiated | 2025-06-11 |
| Enforcement report date | 2025-07-09 |
| FDA classified on | 2025-07-03 |
| Terminated on | 2025-10-28 |
| Distribution | Nationwide |
| Quantity | 40,522 bottles plus 582,000 individual gummies |
| How the firm notified | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| Recall number | H-0212-2025 |
Lots, codes and how to check your bottle
FDA’s “code info” field for this event, verbatim:
1. UPC Code: 4099100290868 Lot #: 248046601 Expiration Date: 10/2026 2. UPC Code: 888670132487 Lot #: 248046601 Expiration Date: 10/2026 3. UPC Code: 850005214670 Lot #: 248046601 Expiration Date: 10/2026 4. Lot# 248046601 Expiration date: 10/2026
Find the lot number on the bottom of the container, beside the seal or on the box flap; the expiration date is usually printed next to it. If the code on your container appears above, it is in scope. If the product name matches but the code does not, your unit is not part of this recall, though a second lot is sometimes added later, so re-check the recall list before finishing the bottle.
Why this is a Class I recall
FDA assigns the class by the probability and severity of harm, not by how much product is involved. For this event the reason falls into what we file as undeclared allergen: the product contains a major food allergen that the label does not declare. For most buyers this is harmless; for someone with that allergy a single serving can be an emergency, which is why FDA treats undeclared peanut, milk, wheat, egg, soy, tree nut, fish, shellfish or sesame as a recall trigger.
FDA’s definition of Class I (21 CFR 7.3) is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. A Class I recall is the strongest signal FDA sends about a consumer product short of a seizure; it is reserved for the cases where continuing to use the product is itself the risk. The reason text is the authority for this specific event; the class is FDA’s summary judgement of it.
If you bought it
- Stop taking it now; for a Class I recall this is the point of the notice.
- Match your lot against the codes above. Keep the container: the firm’s notice normally offers a refund on proof of the lot number or a photo.
- If you or the person taking it has the allergy in question, treat any reaction as you would any exposure to that allergen and tell your doctor. Then report to FDA MedWatch (online form or 1-800-FDA-1088).
- Check the firm’s other products. A recall event often expands to the same firm’s other SKUs a week or two later. Search “Vita Warehouse Corp.” on the full recall list.
A checked alternative for vitamin B12
The product in this recall names Vitamin B12. If you were taking it for that ingredient, the useful next step is a product whose contents can be checked, not a different bottle from the same shelf. Our vitamin B12 guide ranks the products we track by dose per serving, verification and cost per dose. A registry listing (NSF, USP, Informed Sport) is what would have caught an undeclared allergen at the label-audit step; a “tested” claim on the front of the bottle is not.
Frequently asked questions
Why was Welby Vitamin B12 Adult Gummies recalled?
FDA's enforcement report gives the reason as: "Contains undeclared peanut". FDA records the recall type as "Voluntary: Firm initiated"; Vita Warehouse Corp. of Ronkonkoma, NY started it June 11, 2025 and it was posted in FDA's enforcement report on July 9, 2025 as Class I.
Which lots of Welby Vitamin B12 Adult Gummies are affected?
FDA's record lists: 1. UPC Code: 4099100290868 Lot #: 248046601 Expiration Date: 10/2026 2. UPC Code: 888670132487 Lot #: 248046601 Expiration Date: 10/2026 3. UPC Code: 850005214670 Lot #: 248046601 Expiration Date: 10/2026 4. Lot# 248046601 Expiration date: 10/2026. Match these against the lot number, UPC or expiration date printed on your container; a bottle whose code is not listed is not part of this recall.
Where was Welby Vitamin B12 Adult Gummies sold?
FDA's record gives the distribution as: "Nationwide". Quantity recalled: 40,522 bottles plus 582,000 individual gummies.
Is this recall over?
FDA lists the status as "Terminated". Terminated means FDA has decided the firm made all reasonable efforts to retrieve the product; it does not mean bottles already in homes were retrieved, so a matching lot on your shelf is still in scope.
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Sources
- U.S. Food and Drug Administration. Enforcement report, event 97062, recall number H-0212-2025. Via openFDA Food Enforcement API, retrieved September 21, 2026. H-0212-2025
- 21 CFR 7.3(m): recall classification definitions. eCFR Title 21 Part 7.
- FDA. MedWatch: The FDA Safety Information and Adverse Event Reporting Program. fda.gov/safety/medwatch.