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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 84109

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

Open FDA event record

Event summary

Timeline bucket
October 09, 2019
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Medivators, 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

7 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 7

Medivators Endo Smartcap Endoscope Tubing. REF100145. Packaged as Contents 1, 10, 50, and found in BMP-C145. Tubing for Olympus 140/240, 160/260, 180/280, 190/290 Series Endoscopes. Sterile EO - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.

Z-1772-2020
Recall number
Z-1772-2020
Initiated
October 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
Medivators, Inc.
Quantity
53,790 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

Code information

Lot # / UDI #s: 427416 / 00677964059492208051427416, 427098 / 00677964059492208031427098, 427819 / 00677964059492208071427819, 427154 / 00677964059492208031427154.

Distribution pattern

Worldwide distribution - US Nationwide distribution and the countries of Australia, England.

device · product 2 of 7

Medivators Endo Smartcap Endoscope Tubing. REF100145CO2, packaged as Contents 1, 10, 50 and found in BMP-C145CO2. Tubing for Olympus 140/240, 160/260, 180/280, 190/290 Series Endoscopes. Sterile EO - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.

Z-1773-2020
Recall number
Z-1773-2020
Initiated
October 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
Medivators, Inc.
Quantity
53,790 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

Code information

Lot # / UDI #s: 426399 / 006779640594692207241426399, 426401 / 006779640594692207241426401.

Distribution pattern

Worldwide distribution - US Nationwide distribution and the countries of Australia, England.

device · product 3 of 7

Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXTU, packaged as Contents 1, 10, 50. Tubing for Olympus 140/240, 160/260, 180/280, 190/290 Series Endoscopes With Extended CO2 Input. Sterile EO - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.

Z-1774-2020
Recall number
Z-1774-2020
Initiated
October 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
Medivators, Inc.
Quantity
53,790 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

Code information

Lot # / UDI #s: 426407 / 006779640590942207241426407, 427516 / 006779640590942208051427516, 428107 / 006779640590942208081428107, 427865 / 006779640590942208071427865.

Distribution pattern

Worldwide distribution - US Nationwide distribution and the countries of Australia, England.

device · product 4 of 7

Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXT, packaged as Contents 1, 10, 50, and found in BMP-C145CO2EXT. Tubing for Olympus 140/240, 160/260, 180/280, 190/290 Series Endoscopes With Extended CO2 Input. Sterile EO - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.

Z-1775-2020
Recall number
Z-1775-2020
Initiated
October 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
Medivators, Inc.
Quantity
53,790 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

Code information

Lot # / UDI #s: 427118 / 006779640590872208031427118, 427117 / 006779640590872208031427117, 427116 / 006779640590872208031427116, 428819 / 006779640590872208131428819, 430069 /006779640590872208241430069, 426432 / 006779640590872207251426432, 426431 / 006779640590872207251426431, 426433 / 006779640590872207251426433, 427129 / 006779640590872208031427129, 427505 / 006779640590872208051427505, 427132 / 006779640590872208031427132, 428284 / 006779640590872208111428284, 428110 / 006779640590872208081428110, 427130 / 006779640590872208031427130, 427131 / 006779640590872208031427131, 428821 / 006779640590872208131428821, 428823 / 006779640590872208131428823, 428282 / 006779640590872208111428282, 428576 / 006779640590872208121428576, 427119 / 006779640590872208031427119.

Distribution pattern

Worldwide distribution - US Nationwide distribution and the countries of Australia, England.

device · product 5 of 7

Medivators EndoGator REF 100650. Kit for Olympus 140/160/180/190 Series GI Endoscopes forCO2 Connection with Olympus OFP or Boston Scientific Endostat II Irrigation Pump Units. Contents 10. Sterile EO. of 100145CO2EXT Endo SmartCap Irrigation Tubing for Olympus 140/240, 160/260, 180/280, 190/290 Series GI Endoscopes with Extended CO2 Input - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.

Z-1776-2020
Recall number
Z-1776-2020
Initiated
October 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
Medivators, Inc.
Quantity
53,790 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

Code information

Lot # / Case UDI#s: 429694 / 2067796406529722070110429694, 429695 / 2067796406529722060110429695, 430357 / 2067796406529722070110430357, 430566 / 2067796406529722070110430566, 432106 / 2067796406529722080110432106, 431602 / 2067796406529722070110431602, 431611 / 2067796400000722070110431611, 431972 / 2067796406529722070110431972, 432728 / 2067796406529722080110432728, 431833 / 2067796406529722080110431833, 432920 / 2067796406529722080110432920, 432919 / 2067796406529722080110432919.

Distribution pattern

Worldwide distribution - US Nationwide distribution and the countries of Australia, England.

device · product 6 of 7

Medivators EndoGator REF 100651. Kit for Olympus 140/160/180/190 Series GI Endoscopes for CO2 Connection with Endogator EGP-100, Olympus OFP, Olympus AFU-100 & Erbe EIP 2 Irrigation Pump Units. Contents 10. Sterile EO. of 100145CO2EXT Endo SmartCap Irrigation Tubing for Olympus 140/160/180/190 Series GI Endoscopes with Extended CO2 Input - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.

Z-1777-2020
Recall number
Z-1777-2020
Initiated
October 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
Medivators, Inc.
Quantity
53,790 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

Code information

Lot # / Case UDI#s: 430358 / 2067796406530322060110430358, 429884 / 2067796406530322060110429884, 428806 / 2067796406530322070110428806, 430568 / 2067796406530322060110430568, 431254 / 2067796406530322070110431254, 431455 / 2067796406530322070110431455, 431603 / 2067796406530322070110431603, 431834 / 2067796406530322070110431834, 431985 / 2067796406530322070110431985, 431973 / 2067796406530322070110431973, 432922 / 2067796406530322070110432922, 432108 / 2067796406530322070110432108, 432921 / 2067796406530322070110432921, 433116 / 2067796406530322070110433116, 433115 / 2067796406530322080110433115.

Distribution pattern

Worldwide distribution - US Nationwide distribution and the countries of Australia, England.

device · product 7 of 7

Medivators Endo carry-on Procedure Kit REF CPK-100222-0002 - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water source to supply air or CO2 and sterile water to an endoscope during endoscopic procedures.

Z-1778-2020
Recall number
Z-1778-2020
Initiated
October 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
Medivators, Inc.
Quantity
53,790 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Equipment maintenance

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.

Code information

Lot # 1000028736 GTIN: 00677964086045 Use-by date: 210120

Distribution pattern

Worldwide distribution - US Nationwide distribution and the countries of Australia, England.

Field note

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