FDA Enforcement Class II Terminated

Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.

Recall: Z-0631-2019 · Reported December 26, 2018

Enforcement

Recall Number
Z-0631-2019
Event ID
81579
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Cardinal Health 200, LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
December 26, 2018
Initiation Date
October 31, 2018
Classification Date
December 18, 2018
Termination Date
August 12, 2025
Address
3651 Birchwood Dr, Waukegan, IL, 60085-8337, United States

Description

Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a disposable device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.

Reason

Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.

Code Info

Product code: 2D73DP55, Lot Numbers: TS18060249, TS18070244, TS18080021, TS18080344, and TS18090280.

Distribution

Worldwide Distribution: US (Nationwide distribution) to states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY and to countries of: Austria, Belgium, Canada, Chile, Costa Rica, France, Germany, Italy, Luxembourg, Martinique, Monaco, Netherlands, Poland, Reunion, Spain, Sweden, Switzerland, Taiwan, and United Kingdom.

Quantity

1,475,095 pairs total