Recall Z-0456-2019

American Contract Systems, Inc. · initiated December 28, 2016

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

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.

Codes / lots: 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)

Reason for recall

Powdered Surgical Gloves are an FDA banned substance.

FDA-determined cause: Other

Action taken

The firm, ACS, notified Customers via phone call and email on about 12/28/2016. The customers were informed about the product, problem and actions to be taken. The customers were instructed to identify and remove all the affected kits for replacement of the recalled gloves; tray insert label must reflect the omission of the powered gloves; and ban, quarantine and return affected product. If you have any questions, contact that Quality Manager at 816-920-5846 or email to: tbakke@amconsys.com.

Details

Recall number
Z-0456-2019
Initiated
December 28, 2016
Terminated
November 14, 2018
Product code
KGO – Surgeon'S Gloves
Quantity
1,180 kits
Distribution
US Distribution to states of: IL, MO, NE, and OH.
Recalling firm
American Contract Systems, Inc., Kansas City, MO

Official FDA recall record