Recall company profile

Greer Laboratories, Inc. Recalls

Overview of recall records associated with Greer Laboratories, Inc., including dates, categories and classifications where available.

2recall records
Dec 7, 2022latest record date
Dec 7, 2022earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceDec 7, 2022

GREER DIA - KIT ANTIGEN M recall — FDA Z-0348-2023

The product was recalled because stability evaluation of the lots indicated a decrease in reactivity that could lead to a potential false-negative result interpretation. The issue was…

Class IIFDA: TerminatedGreer Laboratories, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Greer Laboratories, Inc. 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.