Class IITerminated in FDA datasetRecall initiated May 19, 2023

Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL)

Recalling firm: Procaps S.A. de C.V.

Why it was recalled

PEG-40 not declared as an ingredient on the label

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 30, 2023.

Check your package

Compare the exact product and package details with the label you have.

ProductBacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 packaged in a bottle inside a cardboard box
Package size8 fl. oz
UPC841548000028

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC841548000028ita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 packaged in a bottle inside a cardboard box

Original FDA recall reason

PEG-40 not declared as an ingredient on the label

Recall details

Recall number
F-0978-2023
Event ID
92385
FDA status
Terminated
Initiated
May 19, 2023
Reported
Jun 14, 2023
Classified
Jun 7, 2023
Terminated
Nov 30, 2023
Quantity
33,684 Boxes
Location
Soyapango, El Salvador
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

DE, TX, CA

FDA source record · F-0978-2023

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.