Home › Device types › LYY
Latex Patient Examination Glove
FDA product code LYY · Class 1 · General Hospital
1,675
Registered devices
3,005
Adverse events
6
Recalls
1,954
510(k) clearances
Devices with this code
latex edition IC — Harps USA, Inc.Uniseal High-Risk Latex — UnisealBLOSSOM — Mexpo International Inc.MICROFLEX — Ansell Healthcare ProductNova — NU RADIANCE INCSAFARI — Mexpo International Inc.SkinGard TPF — MARCON RUBBER INDUSTRY SDN BHDMcKesson — MCKESSON MEDICAL-SURGICAL INC.MICROFLEX — Ansell Healthcare ProductBeesure — ASCEND EAGLE INCORPORATEDDermatec Gold Star — Relda, Llc.Medgluv — Medgluv Inc.Health-Tec/DHP Latex Exam Gloves — Dental Health Products IncBetter Touch — CENTRAL ASSOCIATION FOR THE BLIND, INC.Vitaderm Latex Examination Gloves — TOP QUALITY MANUFACTURING, INC.ProWorks — TRANZONIC COMPANIES, THEBlack Pearl — Ug Healthcare (usa), Inc.Le soothe Latex PF Exam Natural SM — Smarthealth, Inc.AmbiCanner — SUMMIT GLOVE INC.Amtouch - Rely-a-Grip — AMERICAN MEDICAL & HOSPITAL SUPPLY CO., INC.ShieldMaxx — ECON DISPOSABLE SUPPLIES, INCBLOSSOM — Mexpo International Inc.Uniseal BlackSeal Latex — UnisealCranberry — ASCEND EAGLE INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-08-19 | Ansell Healthcare Products LLC | Examination gloves were shipped inadvertently, without to verify barrier integrity. |
| 2011-12-22 | Adenna Inc | The recall was initiated because Adenna Inc. distributed latex gloves that have been FDA refused. |
| 2006-04-10 | Gulf South Medical Supply Inc | FDA's laboratory analysis found holes in the gloves that exceeded the allowable limit. Gloves with holes compromise the integrity of the latex barrier and have |
| 2003-06-27 | Henry Schein, Inc. | FDA's analysis revealed defects (holes) in the latex gloves. |
| 2003-06-27 | Henry Schein, Inc. | FDA's analysis revealed defects (holes) in the latex gloves. |
| 2002-07-23 | American Healthcare Products Inc | Unfit for intended use due to stickiness. |
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