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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81632

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

Open FDA event record

Event summary

Timeline bucket
November 21, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Abbott Ireland Diagnostics Division

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

6 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 6

Alinity i TSH Reagent Kit, List Number 07P4830

Z-0664-2019
Recall number
Z-0664-2019
Initiated
November 21, 2018
Classification
Class II
Status
Terminated
Quantity
678 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Code information

UDI/Lot Numbers: (01)00380740131159 (17)190710(10)90061UI00 / 90061UI00 (01)00380740131159 (17) 190827(10) 91526UI00 / 91526UI00 (01)00380740131159 (17)190924(10)92291UI00 / 92291UI00

Distribution pattern

AR, FL, GA, MD, OK, VA

device · product 2 of 6

Alinity i Free T4 Reagent Kit, List Number 07P7030

Z-0665-2019
Recall number
Z-0665-2019
Initiated
November 21, 2018
Classification
Class II
Status
Terminated
Quantity
294 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Code information

UDI/Lot Numbers (01)00380740121822 (17)190727(10)90111UI00 / 90111UI00 (01)00380740121822 (17)190911(10)92388UI00 / 92388UI00

Distribution pattern

AR, FL, GA, MD, OK, VA

device · product 3 of 6

Alinity i Total Beta-hCG Reagent Kit, List Number 07P5121

Z-0666-2019
Recall number
Z-0666-2019
Initiated
November 21, 2018
Classification
Class II
Status
Terminated
Quantity
27 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Code information

UDI/Lot Numbers (01)00380740160616 (17)190807(10)92056UI00 / 92056UI00

Distribution pattern

AR, FL, GA, MD, OK, VA

device · product 4 of 6

Alinity i Estradiol Reagent Kit, List Number 07P5020

Z-0667-2019
Recall number
Z-0667-2019
Initiated
November 21, 2018
Classification
Class II
Status
Terminated
Quantity
79 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Code information

UDI/Lot Numbers (01)00380740131159 (17)190317(10) 90193UI00 / 90193UI00

Distribution pattern

AR, FL, GA, MD, OK, VA

device · product 5 of 6

Alinity i Progesterone Reagent Kit, List Number 08P3620

Z-0668-2019
Recall number
Z-0668-2019
Initiated
November 21, 2018
Classification
Class II
Status
Terminated
Quantity
157 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Code information

UDI/Lot Numbers (01)00380740121877 (17)190503(10) 91254UI00 / 91254UI00 (01)00380740121877 (17)190618(10)92360UI00 / 92360UI00

Distribution pattern

AR, FL, GA, MD, OK, VA

device · product 6 of 6

Alinity i 25-OH Vitamin D Reagent Kit, List Number 08P4532

Z-0669-2019
Recall number
Z-0669-2019
Initiated
November 21, 2018
Classification
Class II
Status
Terminated
Quantity
760 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Abbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle neck is damaged, it may cause a failure during the reagent loading process on the Alinity i instrument.

Code information

UDI/Lot Numbers (01)00380740121952 (17)191011(10)92313UI00 / 92313UI00 (01)00380740121952 (17)190831(10)92484UI00 / 92484UI00

Distribution pattern

AR, FL, GA, MD, OK, VA

Field note

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