CLASS II Food recall · Reported 14 Jun 2023 · FDA Enforcement Report
Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 recalled
Procaps is recalling Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12, distributed in California, Delaware, Texas. The recall was initiated on 19 May 2023 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-0978-2023
- FDA event ID
- 92385
- Recalling firm
- Procaps, Soyapango
- Brand
- Bacaolinita
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 19 May 2023
- FDA classified
- 7 Jun 2023
- Reported
- 14 Jun 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Allergens
- Product category
- Vitamins
Timeline
| 19 May 2023 | Recall initiated by company | |
| 7 Jun 2023 | Classified by FDA | +19 days |
| 14 Jun 2023 | 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
PEG-40 not declared as an ingredient on the label
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 packaged in a bottle inside a cardboard box
Where it was distributed
DE, TX, CA
Questions about this recall
Why was it recalled?
PEG-40 not declared as an ingredient on the label
Which lots are affected?
Lot #: 1358739, 1379697, 1379718, 1387103, 1404273, 1416127, 1420872, 1423729, 1451962
Where was it sold?
DE, TX, CA
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.
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