Has Abbott Ireland Limited had product recalls?

Yes, 1 recall on file. See the full history below for each one.

Is this FDA enforcement data for Abbott Ireland Limited official?

Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.

How many FDA actions has Abbott Ireland Limited had?

Argus HQ has recorded 1 FDA events for Abbott Ireland Limited: 0 warning letters, 1 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

What is the most recent FDA action against Abbott Ireland Limited?

The most recent FDA event Argus HQ has on file for Abbott Ireland Limited is dated 2023-06-14, with a severity rating of "medium" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

FDA Enforcement History: Abbott Ireland Limited

Here's the summary: Argus HQ has recorded 1 FDA events for Abbott Ireland Limited: 0 warning letters, 1 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2023-06-14 to 2023-06-14. The most severe rating Argus HQ has assigned across this history is "medium". Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

FDA action counts

Total FDA actions	1
Warning letters	0
Recalls	1
Approval records	0
Form 483 inspection citations	0
Most recent action	June 14, 2023

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Abbott Ireland Limited has 1 FDA event on file. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Enforcement history

On 2023-06-14, Argus HQ recorded an FDA recall for Abbott Ireland Limited, rated "medium" severity in Argus HQ's classification: Abbott Ireland Limited — Class III recall: Alinity i Anti-TPO Reagent Kit, List Number 09P3521. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Frequently asked questions

Has Abbott Ireland Limited had product recalls?: Yes, 1 recall on file. See the full history below for each one.
Is this FDA enforcement data for Abbott Ireland Limited official?: Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.
How many FDA actions has Abbott Ireland Limited had?: Argus HQ has recorded 1 FDA events for Abbott Ireland Limited: 0 warning letters, 1 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
What is the most recent FDA action against Abbott Ireland Limited?: The most recent FDA event Argus HQ has on file for Abbott Ireland Limited is dated 2023-06-14, with a severity rating of "medium" in Argus HQ's classification. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

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Abbott Ireland Limited — Class III recall: Alinity i Anti-TPO Reagent Kit, List Number 09P3521 →

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Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Verified from FDA.gov · Last updated: Jun 14, 2023

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2023). FDA Enforcement History: Abbott Ireland Limited. Digital Empire LLC. Retrieved from https://argushq.ai/company/abbott-ireland-limited

MLA

"FDA Enforcement History: Abbott Ireland Limited." Argus HQ Research, Digital Empire LLC, 2023, argushq.ai/company/abbott-ireland-limited.

Chicago

Argus HQ Research. "FDA Enforcement History: Abbott Ireland Limited." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/company/abbott-ireland-limited.

BibTeX

@misc{argushq_argushq_ai_company_abbott_ireland_limited_2023,
  title = {FDA Enforcement History: Abbott Ireland Limited},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/abbott-ireland-limited},
  note = {Accessed: July 17, 2026}
}

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗