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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71727

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

Open FDA event record

Event summary

Timeline bucket
November 21, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Teleflex, Inc.

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

9 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 9

Bronchial Double Lumen Tube Set (Left), Sterile

Z-2407-2015
Recall number
Z-2407-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
6,991 ea. - US & 136,759 ea. - INTL

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 116100260  Batch Number 13GT24, 13HT07, 13IT16, 13KT23, 14AT08, 14DT19, 14ET10, 14ET11, 14FT04, 14FT10, 14GT03; Product Code 116100280  Batch Number 13GT24, 13KT05, 13KT23, 14AT12, 14ET23; Product Code 116100350  Batch Number 13GT24, 13HT07, 13IT16, 13JT08, 13KT05, 13KT18, 13KT23, 13LT14, 14CT06, 14DT10, 14DT19, 14ET23; Product Code 116100370  Batch Number 13GT11, 13GT24, 13HT07, 13IT16, 13JT25, 13KT23, 13LT04, 13LT18, 14CT11, 14DT13, 14DT19, 14DT24, 14DT25, 14ET10, 13ET11; Product Code 116100390  Batch Number 13FT12R, 13HT07, 13IT16, 13JT11, 13JT15, 13JT25, 13KT18, 13KT23, 14AT12R, 14BT09, 14ET10, 14ET11; Product Code 116100410  Batch Number 13FT12R, 13GT05, 13HT07, 13IT20, 13JT25, 13KT05, 13KT18, 13LT18, 14DT19, 14ET04, 14ET10, 14ET11, 14FT05, 14FT10; Product Code 116100-000260  Batch Number 13FT12, 13FT17, 13GT24, 13HT07, 13HT12, 13HT17, 13IT05, 13IT10, 13IT20, 13IT20R, 13JT05R, 13LT04, 14BT15, 14BT16, 14CT16, 14DE14J, 1DT13, 14ET04, 14ET10, 14GT03, 14GT15, 14GT21, 14HT09, 14HT12, 14HT20, 14IT05, 14IT08, 14JT12, 14JT24; Product Code 116100-000280  Batch Number 13GT16, 13GT23, 13HT17, 13IT10, 13IT13, 13IT16, 13IT20, 13IT20R, 13JT08, 13KT05, 13KT18, 13KT23, 14AT08, 14AT12, 14BT16, 14CT06, 14CT11, 14CT16, 14DE14J, 14DT10, 14DT19, 14DT20, 14DT24, 14ET04, 14ET10, 14ET22, 14ET23, 14FT04, 14FT05, 14GT03, 14GT18, 14HT20, 14IT14, 14JT12; Product Code 116100-000350  Batch Number 13FT06, 13FT12, 13FT17, 13FT18, 13GT23, 13GT24, 13HT07, 13HT12, 13HT17, 13IE36R, 13IT05, 13IT10, 13IT16, 13JT08, 13JT11, 13JT25, 13KT05, 13KT12, 13KT18, 13KT23, 13LT04, 13LT14, 14AT08, 14AT16, 14BT15, 14BT21, 14CT11, 14CT16, 14CT20, 14DT10, 14DT13, 14DT15, 14DT19, 14ET04, 14ET05, 14ET22, 14ET23, 14ET28, 14FT04, 14GT05, 14GT10, 14HT09, 14HT12, 14HT17, 14HT20, 14IT05, 14IT17, 14JT04, 14JT09, 14JT12, 14JT21, 14JT24; Product Code 116100-000370  Batch Number 13FT06, 13FT12, 13FT18, 13GE27J, 13GE31J, 13GT05, 13GT11, 13GT16, 13GT24, 13GT29, 13HT07, 13HT12, 13HT17, 13IT05, 13IT10, 13IT16, 13IT20R, 13JT05, 13JT05R, 13JT08, 13JT15, 13JT21, 13KT05, 13KT12, 13KT15, 13LT04, 13LT11, 13LT14, 13LT18, 14AT08, 14AT12, 14AT16, 14AT20, 14BT14, 14BT15, 14BT16, 14CT06, 14CT11, 14CT21, 14DT03, 14DT10, 14DT13, 14DT24, 14DT25, 14ET04, 14ET10, 14ET22, 14ET23, 14ET28, 14FE23J, 14FT04, 14FT05, 14FT10, 14GT03, 14GT05, 14GT10, 14GT15, 14GT18, 14GT23R, 14HT09, 14HT12, 14HT17, 14HT23, 14HT24, 14IT05, 14IT08, 14IT11, 14IT17, 14JT04, 14JT12, 14JT18, 14JT21, 14JT24; Product Code 116100-000390  Batch Number 13FT06, 13FT12, 13FT17, 13FT18, 13GT05, 13GT16, 13GT24, 13GT29, 13HE35, 13HT07, 13HT16, 13HT17, 13IT10, 13IT13, 13JT05, 13JT08, 13JT11, 13JT15, 13JT20, 13JT21, 13JT25, 13KT05, 13KT12, 13KT18, 13KT23, 13LT04, 13LT14, 14BT09, 14BT14, 14BT15, 14BT16, 14BT21, 14CT06, 14CT11, 14CT20, 14DT03, 14DT06, 14DT10, 14DT13, 14DT15, 14DT24, 14DT25, 14EE21J, 14ET04, 14ET10, 14ET22, 14ET28, 14FT04, 14FT05, 14FT10, 14FT13, 14GT03, 14GT05, 14GT15, 14GT18, 14HT03R, 14HT09, 14HT12, 14HT17, 14IT05, 14IT11, 14IT14, 14IT17, 14JT04, 14JT09, 14JT12, 14JT21; Product Code 116100-000410 - Batch Number 13FT06, 13FT12, 13FT18, 13GT05, 13GT11, 13GT16, 13GT23, 13GT29, 13HT07, 13HT12, 13HT17, 13IT05, 13IT10, 13IT16, 13IT20, 13IT20R, 13JT08, 13JT15, 13KT05, 13KT12, 13KT18, 13KT23, 13LT04, 13LT08, 13LT14, 13LT18, 14AT08, 14AT16, 14AT20, 14BT15, 14CT06,14CT11, 14CT16, 14CT20, 14DT06, 14DT10, 14DT13, 14DT24,14EE21J, 14ET04, 14ET05, 14ET10, 14ET22, 14FT10, 14FT13, 14FT16, 14FT20, 14GT05, 14GT15, 14GT18, 14HT03, 14HT09, 14HT17, 14HT24, 14IT05, 14IT08, 14IT17, 14JT09, 14JT12, 14JT21; Product Code 16100-000350  Batch Number 14DE14J, 14FE24J, 14GE28J

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 2 of 9

Bronchial Double Lumen Tube Set (Right), Sterile

Z-2408-2015
Recall number
Z-2408-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 162000260 Batch Number 14CT11; Product Code 116200280 Batch Number 13JT05, 13KT18, 14CT11, 14FT05, 14FT10; Product Code 116200350 Batch Number 13FT12R, 13GT11, 13HT07, 13KT23, 14AT08; Product Code 116200370 Batch Number 13KT23, 13LT14, 14DT25, 14ET23; Product Code 116200390 Batch Number 13HT12, 13JT08, 13KT18, 14ET10; Product Code 116200410 Batch Number 14ET05, 14ET22; Product Code 116201350 Batch Number 13FT12R, 13GT05; Product Code 116201410 Batch Number 14ET04; Product Code 116200-000260 Batch Number 13FT12, 13GE29J, 13GT29, 13HT12, 13HT17, 13IT10, 13JT05R, 13JT21, 13LT04, 14DT03, 14ET04, 14ET10, 14ET22, 14FT04, 14GT11, 14GT18, 14GT21, 14HT09, 14HT17; Product Code 116200-000260 - Batch Number 13FT12, 13GE29J, 13GT29, 13HT12, 13HT17, 13IT10, 13JT05R, 13JT21, 13LT04, 14DT03, 14ET04, 14ET10, 14ET22, 14FT04, 14GT11, 14GT18, 14GT21, 14HT09, 14HT17; Product Code 116200-000280 Batch Number 13FT06, 13FT12, 13GE29J, 13HT12, 13HT17, 13IT10, 13JT11, 13KT05, 13KT18, 13LT11, 14CT06, 14CT21, 14DT10, 14DT24, 14ET10, 14ET22, 14FT04, 14FT10, 14GT03, 14GT15, 14GT21, 14HT09, 14IT05, 14IT20; Product Code 116200-000350 Batch Number 13GE28J, 13GT05, 13GT11, 13GT23, 13GT29, 13HT07, 13HT12, 13HT17, 13IT10, 13IT13, 13JT08, 13JT20, 13JT21, 13KT05, 13KT12, 13KT23, 13LT04, 13LT08, 13LT11, 14AT04, 14AT08, 14BT21, 14CT06, 14CT16, 14CT20, 14CT21, 14DT06, 14DT24, 14ET04, 14ET05, 14FT22, 14FT04, 14FT10, 14FT13, 14FT20, 14GT05, 14GT15, 14HT09, 14HT20, 14HT23, 14IT05, 14IT08, 14JT09, 14JT12, 14JT24; Product Code 116200-000370 Batch Number 13FT17, 13GE28J, 13GT05, 13GT16, 13HT12, 13IT05, 13IT10, 13IT16, 13IT20R, 13JT08, 13JT15, 13KT05, 13KT12, 13KT23, 13LT08, 13LT14, 14AT08, 14AT12, 14BT21, 14CT06, 14CT16, 14DT03, 14DT13, 14DT19, 14DT20, 14DT24, 14DT25, 14ET05, 14ET23, 14ET28, 14FT04, 14FT13, 14FT20, 14GT03, 14GT18, 14HT03, 14HT09, 14HT12, 14HT17, 14IT08, 14IT17, 14JT21, 14JT24; Product Code 116200-000390 Batch Number 13FT12, 13FT18, 13GE28J, 13GT16, 13GT29, 13HT12, 13IT05, 13IT10, 13IT13, 13IT20, 13IT20R, 13JT05R, 13JT08, 13JT15, 13JT20R, 13KT05, 13KT18, 13LT08, 14BT15, 14BT16, 14BT21, 14CT11, 14CT16, 14DT13, 14DT15, 14ET04, 14ET10, 14FT04, 14FT16, 14GT03, 14GT15, 14GT21, 14HT03, 14HT17, 14HT23, 14IT05, 14IT08, 14IT17, 14IT20, 14JT12, 14JT24; Product Code 116200-000410 Batch Number 13FT12, 13GE30J, 13GT11, 13GT24, 13GT29, 13HT12, 13HT17, 13IT10, 13IT13, 13IT20R, 13JT05, 13JT05R, 13JT20, 13KT05, 13KT12, 13LT04, 13LT08, 14AT08, 14BT21, 14CT11, 14DT13, 14DT15, 14DT19, 14DT24, 14ET04, 14ET05, 14ET22, 14FT13, 14GT15, 14GT21, 14HT03, 14HT09, 14HT17, 14HT20, 14HT23, 14IT08

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 3 of 9

Bronchial One Lumen Tube - Left

Z-2409-2015
Recall number
Z-2409-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 115900-000065 Batch Number 13FT06, 13GT24, 13JT08, 13KT12, 13LT08, 14AT20, 14DT19, 14ET04, 14GT10, 14GT15, 14IT11, 14JT09, 14JT24; Product Code 115900-000080 Batch Number 13FT17, 13IT11, 13KT05, 13KT12, 14AT04, 14BT04, 14BT15, 14DT19, 14ET04, 14ET22, 14GT15, 14GT18, 14IT14, 14JT09, 14JT18

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 4 of 9

Bronchial One Lumen Tube - Right

Z-2410-2015
Recall number
Z-2410-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 115901-000065 Batch Number 13FT06, 13IT05, 13JT08, 13KT12, 14CT11, 14DT03, 14DT24, 14ET04, 14FT04, 14FT20, 14GT10; Product Code 115901-000080 - Batch Number 13GT16, 13KT18, 13LT08, 14CT11, 14DT03, 14DT24, 14GT15, 14HT12, 14HT20, 14JT04, 14JT12, 14JT21

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 5 of 9

Carlens Bronchial Double Lumen Tube Set (Left) Sterile

Z-2411-2015
Recall number
Z-2411-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 116101370  Batch Number 13KT12, 13LT04; Product Code 116101390  Batch Number 13KT18; Product Code 116101410  Batch Number 13FT12R, 13GT05, 13JT11, 13JT15; Product Code 116101-000350  Batch Numbers 14JT14; Product Code 116101-000370  Batch Numbers 13FT06, 13FT12, 13FT18, 13GT05, 13GT29, 13HT07, 13HT12, 13HT17, 13IT16, 13IT20R, 13JT08, 13JT21, 13KT12, 13KT18, 13LT04, 13LT14, 14AT08, 14BT14, 14BT15, 14CT11, 14CT16, 14DT10, 14DT15, 14DT19, 14DT24, 14ET10, 14ET11, 14ET22, 14FT04, 14FT05, 14FT10, 14FT13, 14GT10, 14GT11, 14GT15, 14GT21, 14HT17, 14IT05, 14IT11, 14JT09, 14JT14; Product Code 116101-000390  Batch Numbers 13FT06, 13FT12, 13GT05, 13GT23, 13GT29, 13HE35, 13HT17, 13IT05, 13IT16, 13IT20, 13IT20R, 13JT08, 13JT21, 13KT12, 13KT15, 13KT18, 13LT04, 13LT11, 14BT14, 14BT21, 14CT11, 14CT21, 14DT03, 14DT13, 14DT15, 14DT19, 14DT20, 14DT25, 14ET04, 14ET28, 14FT04, 14FT16, 14GT10, 14GT11, 14GT21, 14GT23R, 14HT17, 14HT23, 14HT24, 14IT08, 14JT09, 14JT12; Product Code 116101-000410 - Batch Number 13FT06, 13FT12, 13GT05, 13GT24, 13GT29, 13HT07, 13HT12, 13HT17, 13IT16, 13IT20R, 13JT08, 13JT11, 13JT15, 13JT21, 13KT12, 13KT15, 13KT23, 13LT08, 13LT14, 13LT18, 14AT20, 14BT21, 14CT11, 14CT16, 14CT20, 14DT13, 14DT19, 14ET05, 14ET10, 14ET28, 14FT13, 14FT16, 14GT15, 14GT18, 14GT21R, 14HT03, 14HT17, 14HT23, 14HT24, 14JT09

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 6 of 9

Tracheopart Set (Left), Sterile

Z-2412-2015
Recall number
Z-2412-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Produce Code 116400-000750  Batch Number 13FT06, 13GE28J, 13GE31J, 13GT11, 13GT29, 13IT05, 13IT16, 13JT11, 13JT21R, 13JT25R, 13KT05R, 13LT11, 14BT09, 14BT15, 14CT16, 14CT20, 14DE16J, 14DT19, 14FE24J, 14FT16, 14GE29J, 14GT03, 14GT23, 14HT03, 14HT23, 14IT05, 14IT17; Product Code 116400-000850  Batch Number 13FT18, 13GE31J, 13GT05, 13HT17, 13IT13, 13JT15, 13JT20, 13JT20R, 13KT23R, 13LT08, 14BT09, 14BT15, 14CT16, 14CT20, 14DE15J, 14DT08, 14FE24J, 14FT13, 14GE28J, 14GT18, 14GT21, 14HT09, 14IT05, 14IT14, 14JT04, 14JT12; Product Code 116400-000950  Batch Number 13GE30J, 13GT29, 13HT16, 13IT13, 13LT08, 14AE05J, 14DT10, 14ET11, 14FT04, 14GT21, 14IT08, 14IT14, 14JE43J, 14JT18, 14JT24

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 7 of 9

Tracheopart Set (Right), Sterile

Z-2413-2015
Recall number
Z-2413-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 116401-000750  Batch Number 13FT06, 13GT24, 13JT21, 13IT21R, 13KT23, 13KT23R, 14CT21, 14ET11, 14ET22, 14ET28, 14FT16, 14GT15, 14GT23, 14IT17, 14JT18; Product Code 116401-000850  Batch Number 13IT05, 13IT21R, 13KT05, 13LT08, 14CT16, 14DT19, 14ET10, 14ET22, 14FT16, 14GT05, 14GT18, 14HT03, 14HT09; Product Code 116401-000950  Batch Number 13JT21R, 14CT06, 14CT16, 14DT20, 14ET23, 14FT04, 14GT05, 14GT18, 14HT17, 14IT08

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 8 of 9

White Bronchial Double Lumen Tube Set (Right) Sterile

Z-2414-2015
Recall number
Z-2414-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 116201-000350 Batch Number 13FT17, 13GT05, 13GT24, 13HT07, 13HT12, 13HT17, 13IT16, 13IT20, 13JT20, 13JT21, 13JT25R, 13KT05, 13KT05R, 13KT12, 13KT23, 13LT08, 14CT06, 14CT11, 14CT20, 14DT03, 14DT06, 14DT19, 14ET10, 14ET23, 14ET28, 14FT04, 14FT05, 14FT13, 14FT16, 14GT18, 14GT21, 14HT03, 14HT17, 14HT24, 14IT08, 14JT14, 14JT21; Product Code 116201-000370 Batch Number 13FT06, 13GT11, 13GT29, 13HT12, 13HT17, 13IT10, 13IT16, 13IT20R, 13JT08, 13JT20, 13JT25, 13KT05, 13KT12, 13KT23, 13LT08, 13LT11, 14AT08, 14CT06, 14CT11, 14CT20, 14DT19, 14DT24, 14ET04, 14ET10, 14ET22, 14ET23, 14FT04, 14FT13, 14GT18, 14GT21, 14HT03, 14HT20, 14HT23, 14IT05, 14IT08, 14JT14, 14JT18; Product Code 116201-000390 Batch Number 13FT06, 13GT11, 13HT07, 13HT12, 13IT10, 13IT16, 13IT20, 13IT20R, 13JT08, 13JT08R, 13JT20, 13JT21, 13KT12, 13KT18, 14BT16, 14CT06, 14CT16, 14CT20, 14DT03, 14DT13, 14DT24, 14ET10, 14ET23, 14ET28, 14FT13, 14FT16, 14GT05, 14GT18, 14GT21, 14HT03, 14HT09, 14HT20, 14HT23, 14IT08, 14IT14; Product Code 116201-000410 Batch Number 13IT20, 13JT25R, 13KT05R, 13KT12, 13KT15, 13KT18, 13LT11, 14AT08, 14CT11, 14CT16, 14CT21, 14DT13, 14DT19, 14ET04, 14ET22, 14ET28, 14GT18, 14HT03, 14HT17, 14JT12

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago

device · product 9 of 9

Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile

Z-2415-2015
Recall number
Z-2415-2015
Initiated
November 21, 2014
Classification
Class II
Status
Terminated
Recalling firm
Teleflex, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Customer complaints reporting that the cobb connector detached from the main connector prior to use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Customer complaints reporting that the cobb connector detached from the main connector prior to use.

Code information

Product Code 116164-000390  Batch Number 14BT21

Distribution pattern

AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago