Reported Sep 9, 2020 · Completed

PROTEXIS Latex Micro Surgical Gloves Size 6.5 - 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 6.5 -
  • 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
    • 2D72NT65X Lot #: TS19060064
    • TS19060158
    • TS19060303
    • TS19060393
    • TS19070019
    • TS19070068
    • TS19070138
    • TS19070185
    • TS19070297
    • TS19080022
    • TS19080051
    • TS19080128
    • TS19080134
    • TS19080239
    • TS19080326
    • TS19090058
    • TS19090104
    • TS19090212
    • TS19090295
    • TS19100043
    • TS19100138
    • TS19100173
    • TS19100310
    • TS19110023
    • TS19110083
    • TS19110150
    • TS19110211
    • TS19110349
    • TS20020024
    • TS20020262
    • TS20030066
    • TS20030179
    • TS20030219
    • TS20030318
    • TS20040116
  • Additional Affected Lots as of 10/20/20
    • TS20040111
    • TS20040069
    • TS20040104
    • TS20040174
    • TS20040293
    • TS20050140
    • TS20050181
    • TS20050182
    • TS20050268
    • TS20050269
    • TS20050336
    • TS20050344
    • TS20050378
    • TS20060010
    • TS20060064
    • TS20060065
    • TS20060138
    • TS20060140
    • TS20060224
    • TS20060225
    • TS20060285
    • TS20060286
    • TS20070003
    • TS20070081
  • Additional Affected Lots as of 2/23/21TS20070179
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, 6:49 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.