American Contract Systems, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0456-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product 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.

Product Classification:

Class II

Date Initiated: December 28, 2016

Date Posted: November 21, 2018

Recall Number: Z-0456-2019

Event ID: 80754

Reason for Recall:

Powdered Surgical Gloves are an FDA banned substance.

Status: Terminated

Product Quantity: 1,180 kits

Code Information:

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 Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated