Exact FDA event identifier

Event 86131

8 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: July 29, 2020
Product types: Device
Classifications: Class II
Statuses: Completed
Recalling firm wording: Cardinal Health 200, LLC

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

8 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 8

PROTEXIS Latex Micro Surgical Gloves Size 5.5 - 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.

Z-2912-2020

Recall number: Z-2912-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Item Code: 2D72NT55X Lot #: TS19060338, TS19070077, TS19070176, TS19090164, TS19090248, TS19100272, TS19110080, TS20010146, TS20020202, TS20040092 Additional Affected lots as of 10/20/20: TS20040247, TS20050050, TS20050051, TS20050261, TS20060112, TS20060113, TS20070125

Distribution pattern

US Nationwide distribution

device · product 2 of 8

PROTEXIS Latex Micro Surgical Gloves Size 6.0 - 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.

Z-2913-2020

Recall number: Z-2913-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Item Code: 2D72NT60X Lot #: TS19060043, TS19060123, TS19060199, TS19070005, TS19070027, TS19070067, TS19070130, TS19070179, TS19070273, TS19080030, TS19090067, TS19090158, TS19090226, TS19090289, TS19110333, TS19120019, TS19120322, TS20020121, TS20030015, TS20030324 Additional Affected Lots as of 10/20/20: TS20040173, TS20040249, TS20040257, TS20040333, TS20050052, TS20050069, TS20050152, TS20050153, TS20050196, TS20050197, TS20050334, TS20050335, TS20060011, TS20060053, TS20060054, TS20060115, TS20060116, TS20060199, TS20060200, TS20060250, TS20070023, TS20070108, TS20070183

Distribution pattern

US Nationwide distribution

device · product 3 of 8

PROTEXIS Latex Micro Surgical Gloves Size 6.5 - 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.

Z-2914-2020

Recall number: Z-2914-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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 2/23/21: TS20070179

Distribution pattern

US Nationwide distribution

device · product 4 of 8

PROTEXIS Latex Micro Surgical Gloves Size 7.0 - 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.

Z-2915-2020

Recall number: Z-2915-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Item Code: 2D72NT70X Lot #: TS19060339, TS19070029, TS19070108, TS19070180, TS19070285, TS19080035, TS19080064, TS19080140, TS19080186, TS19080271, TS19090054, TS19090149, TS19090266, TS19100058, TS19100107, TS19100186, TS19100308, TS19110038, TS19110090, TS19110157, TS19110225, TS19120005, TS20030299, TS20040046 Additional Affected Lots as of 10/20/20: TS20040204, TS20040260, TS20040312, TS20050113, TS20050157, TS20050289, TS20050290, TS20050391, TS20060093, TS20060152, TS20060153, TS20060204, TS20060237, TS20060238, TS20060296, TS20060304, TS20060305, TS20070020, TS20070107

Distribution pattern

US Nationwide distribution

device · product 5 of 8

PROTEXIS Latex Micro Surgical Gloves Size 7.5 - 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.

Z-2916-2020

Recall number: Z-2916-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

US Nationwide distribution

device · product 6 of 8

PROTEXIS Latex Micro Surgical Gloves Size 8.0 - 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.

Z-2917-2020

Recall number: Z-2917-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Item Code: 2D72NT80X Lot #: TS19060095, TS19060169, TS19060328, TS19060357, TS19070100, TS19080183, TS19080225, TS19080308, TS19090043, TS19090188, TS19090292, TS19100150, TS19100214, TS19100282, TS19110050, TS19110115, TS19110295, TS19110334, TS19120049, TS20050165 Additional Affected Lots as of 10/20/20: TS20040334, TS20040358, TS20040359, TS20050106, TS20050322, TS20060026, TS20060084

Distribution pattern

US Nationwide distribution

device · product 7 of 8

PROTEXIS Latex Micro Surgical Gloves Size 8.5 - 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.

Z-2918-2020

Recall number: Z-2918-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Item Code: 2D72NT85X Lot #: TS19060044, TS19060122, TS19060189, TS19080111, TS19080184, TS19080227, TS19090008, TS19090127, TS19100079, TS19100220, TS19110109, TS19110285, TS19110331, TS19120316, TS20050031, TS20050139 Additional Affected Lots as of 10/20/20: TS20050169, TS20050262, TS20060005

Distribution pattern

US Nationwide distribution

device · product 8 of 8

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.

Z-2919-2020

Recall number: Z-2919-2020
Initiated: July 29, 2020
Classification: Class II
Status: Completed
Recalling firm: Cardinal Health 200, LLC
Quantity: 7119625 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

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

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

US Nationwide distribution