Reported Sep 9, 2020 · Completed

PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: This surgeon s glove is a disposable device made of…

Cardinal Health 200, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337

Is this the product you have?

  • PROTEXIS Latex Micro Surgical Gloves Size 7.5 -
  • Product UsageThis surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensitivity or durability depending on need
Lot codes and dates
  • Item Code
    • 2D72NT75X Lot #: TS19060031
    • TS19060065
    • TS19060168
    • TS19060302
    • TS19080080
    • TS19080176
    • TS19080203
    • TS19080262
    • TS19090027
    • TS19090064
    • TS19090167
    • TS19090272
    • TS19100111
    • TS19100197
    • TS19100244
    • TS19100262
    • TS19110041
    • TS19110102
    • TS19110176
    • TS19110238
    • TS19120002
    • TS19120044
    • TS19120274
    • TS20020286
    • TS20030288
    • TS20040030
    • TS20040086
    • TS20050114
  • Additional Affected Lots as of 10/20/20
    • TS20040051
    • TS20040075
    • TS20040058
    • TS20040176
    • TS20040280
    • TS20040281
    • TS20040291
    • TS20050010
    • TS20050174
    • TS20050306
    • TS20050353
    • TS20060032
    • TS20060038
    • TS20060120
    • TS20060174
    • TS20060175
    • TS20060260
    • TS20050250
Amount recalled
7119625 total

This recall covers 8 products

The agency filed one notice per product. You are reading one of them; the other 7 are below.

Where it was sold

  • Nationwide

Why it was recalled

A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:29 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.