Recall Z-1381-2021— HUBO INTERNATIONAL INC

Name: FDA recall Z-1381-2021
Creator: U.S. Food and Drug Administration
Published: 2020-10-23

Class II · Ongoing

Class II FDA medical device recall by HUBO INTERNATIONAL INC, initiated 2020-10-23. It names one FDA 510(k) clearance: K151208. Product: VGlove NITRILE *** Protect Your Life 100 Patient examination gloves. Reason: Package labeled as nitrile gloves, contains latex gloves..

Recalling firm: HUBO INTERNATIONAL INC
Classification: Class II
Status: Ongoing
Initiated: 2020-10-23
Firm location: South El Monte, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K151208 — Powder Free Nitrile Examination GloveVrg Khai Hoan Joint Stock Company·cleared 2015-09-14

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

VGlove NITRILE *** Protect Your Life 100 Patient examination gloves

Reason for recall

Package labeled as nitrile gloves, contains latex gloves.

Data sourced from openFDA. This site is unofficial and independent of the FDA.