Bacaolinita Liquid Supplement (Procaps) – undeclared ingredient (2023)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Procaps S.A. de C.V.
Lot Codes / Batch Numbers
Lot #: 1358739, 1379697, 1379718, 1387103, 1404273, 1416127, 1420872, 1423729, 1451962
Products Sold
Lot #: 1358739, 1379697, 1379718, 1387103, 1404273, 1416127, 1420872, 1423729, 1451962
Procaps S.A. de C.V. is recalling Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 due to PEG-40 not declared as an ingredient on the label. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
PEG-40 not declared as an ingredient on the label
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, DE, TX
Page updated: Jan 6, 2026