Food Recall Check
Class II · Moderate risk Terminated Initiated May 19, 2023 (3 years ago)

Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 recall

Recalled by Procaps S.A. de C.V. · Soyapango, El Salvador

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

PEG-40 not declared as an ingredient on the label

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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

Quantity: 33,684 Boxes

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot #: 1358739, 1379697, 1379718, 1387103, 1404273, 1416127, 1420872, 1423729, 1451962

Where it was sold

California Delaware Texas

FDA's distribution note: DE, TX, CA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Procaps S.A. de C.V.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 19, 2023
In FDA report of
Jun 14, 2023
Terminated
Nov 30, 2023
FDA recall number
F-0978-2023 · event 92385
Official record
FDA enforcement report search

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