Skip to content
Recall Observatory FDA recall evidence

Device product

Protexis Neoprene Surgical Glove, Size 8.0 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.

Z-0636-2019

October 31, 2018

Class II

Product summary

Firm
Cardinal Health 200, LLC
Event
Event 81579
Status
Terminated
Classification
Class II
Quantity
1,475,095 pairs total
Official record key
device-enforcement:Z-0636-2019

Official wording

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 information: Product code: 2D73DP80, Lot Numbers: TS18060134, TS18060230, TS18060323, TS18070039, TS18070313, TS18070372, TS18080027, TS18080351, TS18090164, TS18090218, and TS18090289.

Distribution pattern: 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.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    label in error