Z-0635-03

Latex examination gloves, Uniseal brand

Name: Z-0635-03 Latex examination gloves, Uniseal brand
Creator: American Healthcare Products Inc
Published: 2002-07-23
License: https://open.fda.gov/license/

American Healthcare Products Inc / initiated 2002-07-23 / Terminated

FDA source

American Healthcare Products Inc began a recall of Latex examination gloves, Uniseal brand on 2002-07-23. The reason FDA records is "Unfit for intended use due to stickiness". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0635-03
Status: Terminated
Initiated: 2002-07-23
Posted: 2003-03-12
Terminated: 2005-01-24
Recalling firm: American Healthcare Products Inc
Product: Latex examination gloves, Uniseal brand.
Product code: LYY Latex Patient Examination Glove
Reason for recall: Unfit for intended use due to stickiness.
FDA root cause: Other
Action: Firm sent recall letter 7/23/2002.
Quantity in commerce: 6121 cases
Distribution: Nationwide.
Product codes and lots: Lot numbers: 41991221 41991223 41001105 41001120 41010428 41010530 41010613 41010618

Product code LYY

K945164Class IMultipleProtection Gloves Sdn. Bhd. / cleared 1995-02-03

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)