FDA Enforcement Class II Terminated

Powdered Surgical Gloves, labeled as: a. Baxter and Ansell brand Powdered Surgical Gloves b. Powdered Surgical Gloves included in ACS surgical convenience kits Health care personnel rely on medical gloves as barriers against transmission of infectious diseases and contaminants when conducting surgery, as well as when conducting more limited interactions with patients.

Recall: Z-0456-2019 · Reported November 21, 2018

Enforcement

Recall Number
Z-0456-2019
Event ID
80754
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
American Contract Systems, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
November 21, 2018
Initiation Date
December 28, 2016
Classification Date
November 13, 2018
Termination Date
November 14, 2018
Address
2610 Ne Industrial Dr Ste 220, Kansas City, MO, 64117-2648, United States

Description

Powdered Surgical Gloves, labeled as: a. Baxter and Ansell brand Powdered Surgical Gloves b. Powdered Surgical Gloves included in ACS surgical convenience kits Health care personnel rely on medical gloves as barriers against transmission of infectious diseases and contaminants when conducting surgery, as well as when conducting more limited interactions with patients.

Reason

Powdered Surgical Gloves are an FDA banned substance.

Code Info

Tray Number (Powdered Glove code): MHCE23D (ANS5711104), MHAP41D (ANS7825), MHOC43C (ANS7825), MHPO42D (ANS7825), GVTH071 (ANS5711104), GVTK05L (ANS5711104), GVTK05M (ANS5711104), CXTR68D (ANS5711105), MDEY35H (BAX2D7202I), MDEY35I (BAX2D7202I), FHLV24 (ANS5711105, ANS5711101), LKCA02A (ANS5710503), WIDE32 (ANS7824), UTLU70F (ANS7825), FIOH02H (BAX2D7254)

Distribution

US Distribution to states of: IL, MO, NE, and OH.

Quantity

1,180 kits