RecallRadar

FDA Device recall Z-2919-2020

PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or…

On 2020-09-09 the FDA classified a Class II recall of PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or… by Cardinal Health 200, citing A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2919-2020
ClassificationClass II
Statuscompleted
Initiated2020-07-29
Published2020-09-09
Last updated2026-09-13 11:55 UTC
CompanyCardinal Health 200
DistributionUS

Product

PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: This 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.

Reason

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

Identifiers

code_info
Item Code: 2D72NT90X Lot #: TS19080275, TS19090162, TS19090231, TS20010216, TS20030153 Additional Affected Lots of…Item Code: 2D72NT90X Lot #: TS19080275, TS19090162, TS19090231, TS20010216, TS20030153 Additional Affected Lots of as 10/20/20: TS20040290, TS20050032, TS20060107 Additional Affected Lots as of 2/23/21: TS20040344

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2919-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.