Recall company profile

Bioseal Corporation Recalls

Overview of recall records associated with Bioseal Corporation, including dates, categories and classifications where available.

4recall records
May 26, 2021latest record date
Aug 19, 2020earliest record date

Recall history in this database

Classification mix: Class II: 4.

Medical DeviceMay 26, 2021

Bioseal recall — FDA Z-1624-2021

Pre-op skin prep component ChloraPrep included within kits may allow the growth of Aspergillus penicillioides, which may penetrate the packaging resulting in a breach of the package…

Class IIFDA: CompletedBioseal Corporation
Medical DeviceMay 26, 2021

Bioseal recall — FDA Z-1622-2021

Pre-op skin prep component ChloraPrep included within kits may allow the growth of Aspergillus penicillioides, which may penetrate the packaging resulting in a breach of the package…

Class IIFDA: CompletedBioseal Corporation
Medical DeviceMay 26, 2021

Bioseal recall — FDA Z-1623-2021

Pre-op skin prep component ChloraPrep included within kits may allow the growth of Aspergillus penicillioides, which may penetrate the packaging resulting in a breach of the package…

Class IIFDA: CompletedBioseal Corporation

Understanding this recall history

This page summarizes recall records in which the official source identifies Bioseal Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.