CLASS II Food recall · Reported 16 Feb 2022 · FDA Enforcement Report
Caffeine 125 mg with B6 and B12 vitamins (supplement) recalled
ULTRAtab Laboratories is recalling Caffeine 125 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc, distributed in Florida, New York. The recall was initiated on 6 Oct 2021 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-0723-2022
- FDA event ID
- 89512
- Recalling firm
- ULTRAtab Laboratories, Highland, NY
- Brand
- Caffeine
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Oct 2021
- FDA classified
- 9 Feb 2022
- Reported
- 16 Feb 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Product category
- Vitamins
Timeline
| 6 Oct 2021 | Recall initiated by company | |
| 9 Feb 2022 | Classified by FDA | +126 days |
| 16 Feb 2022 | 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
cGMP Deviations
Product as listed by the FDA
Caffeine 125 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY
Where it was distributed
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Questions about this recall
Why was it recalled?
cGMP Deviations
Which lots are affected?
Product Codes: M960L Bulk Lots: 19E021, 19E022
Where was it sold?
Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
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 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 products in this recall event
8 other products · FDA event 89512This product is part of a recall event; the main page for the event is Electrolyte tablet (Calcium 10.8mg, Potassium 40mg recalled.
More recalls from ULTRAtab Laboratories
All 43Other Vitamins recalls
All 294| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | FulviLife Complex recalled by Wellnov SupplementsFulviLife Complex | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid recalledLiposomal D3-5000IU | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Joint Nourish recalled by Wellnov SupplementsJoint Nourish | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Liposomal Mens Liquid Multivitamin Drops recalled by Wellnov SupplementsLiposomal Mens | Wellnov Supplements | Botulism | Nationwide |
| Food | CLASS II | Liposomal Womens 50+ Liquid Multivitamin Drops recalledLiposomal Womens | Wellnov Supplements | Botulism | Nationwide |