Z-2466-2010

Life Brand Regular Absorbency 40 Count Unscented Plastic Applicator Tampons

Name: Z-2466-2010 Life Brand Regular Absorbency 40 Count Unscented Plastic Applicator Tampons
Creator: First Quality Hygienic Inc
Published: 2010-03-25
License: https://open.fda.gov/license/

First Quality Hygienic, Inc. / initiated 2010-03-25 / Terminated / root cause: labeling and UDI

FDA source

First Quality Hygienic Inc began a recall of Life Brand Regular Absorbency 40 Count Unscented Plastic Applicator Tampons on 2010-03-25. The reason FDA records is "Life Brand Regular Absorbency 40 Count Unscented Plastic Applicator Tampons package contained Super Plus Unscented Plastic Applicator Tampons". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-2466-2010
Status: Terminated
Initiated: 2010-03-25
Posted: 2010-09-22
Terminated: 2010-10-06
Recalling firm: First Quality Hygienic, Inc.
Product: Life Brand Regular Absorbency 40 Count Unscented Plastic Applicator Tampons
Product code: HEB Tampon, Menstrual, Unscented
Reason for recall: Life Brand Regular Absorbency 40 Count Unscented Plastic Applicator Tampons package contained Super Plus Unscented Plastic Applicator Tampons.
Root cause tag: labeling and UDI
FDA root cause: Labeling mix-ups
Action: Consignees were notified via telephone and letter of the need to withdraw product from the market and requested to return all product to manufacturer.
Quantity in commerce: 195 Cases/2340 Cartons
Distribution: Canada
Product codes and lots: Lot 09DPC24P UPC #0-57800-23314-5

Product code HEB

K023479Class IIFemtex Tampons and Other Private Label Plastic Applicator Tampons; Consumer Packages and Bulk PackagesFirst Quality Hygienic, Inc. / cleared 2002-11-26

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)