How many FDA actions has Abbott Diagnostics Scarborough, Inc. had?

Argus HQ has recorded 7 FDA events for Abbott Diagnostics Scarborough, Inc.: 0 warning letters, 7 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 Diagnostics Scarborough, Inc.?

The most recent FDA event Argus HQ has on file for Abbott Diagnostics Scarborough, Inc. is dated 2026-03-25, with a severity rating of "high" 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.

Does Argus HQ track new FDA actions for Abbott Diagnostics Scarborough, Inc. automatically?

Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Abbott Diagnostics Scarborough, Inc. is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for Abbott Diagnostics Scarborough, Inc.?

7 total: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.

Regulatory Record: Abbott Diagnostics Scarborough, Inc.

FDA action counts

Total FDA actions	7
Warning letters	0
Recalls	7
Approval records	0
Form 483 inspection citations	0
Most recent action	March 25, 2026

The short version: Argus HQ has recorded 7 FDA events for Abbott Diagnostics Scarborough, Inc.: 0 warning letters, 7 recalls, 0 approvals, and 0 inspection 483 observations. These events span from 2025-04-23 to 2026-03-25. The most severe rating Argus HQ has assigned across this history is "high". 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.

Enforcement history

On 2026-03-25, Argus HQ recorded an FDA recall for Abbott Diagnostics Scarborough, Inc., rated "high" severity in Argus HQ's classification: Abbott Diagnostics Scarborough, Inc. — Class II recall: Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software…. On 2025-04-23, Argus HQ recorded an FDA recall for Abbott Diagnostics Scarborough, Inc., rated "high" severity in Argus HQ's classification: Abbott Diagnostics Scarborough, Inc. — Class II recall: Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T…. On 2025-04-23, Argus HQ recorded an FDA recall for Abbott Diagnostics Scarborough, Inc., rated "high" severity in Argus HQ's classification: Abbott Diagnostics Scarborough, Inc. — Class II recall: Brand Name: ID NOW RSV 24T Product Name: ID NOW RSV 24T Model/Catalog Number: 43…. On 2025-04-23, Argus HQ recorded an FDA recall for Abbott Diagnostics Scarborough, Inc., rated "high" severity in Argus HQ's classification: Abbott Diagnostics Scarborough, Inc. — Class II recall: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/…. On 2025-04-23, Argus HQ recorded an FDA recall for Abbott Diagnostics Scarborough, Inc., rated "high" severity in Argus HQ's classification: Abbott Diagnostics Scarborough, Inc. — Class II recall: Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T…. On 2025-04-23, Argus HQ recorded an FDA recall for Abbott Diagnostics Scarborough, Inc., rated "high" severity in Argus HQ's classification: Abbott Diagnostics Scarborough, Inc. — Class II recall: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/…. On 2025-04-23, Argus HQ recorded an FDA recall for Abbott Diagnostics Scarborough, Inc., rated "high" severity in Argus HQ's classification: Abbott Diagnostics Scarborough, Inc. — Class II recall: Brand Name: ID NOW RSV 24T Product Name: ID NOW RSV 24T Model/Catalog Number: 43….

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Abbott Diagnostics Scarborough, Inc. has 7 separate FDA recalls on file, more than a single isolated recall event. 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.

Frequently asked questions

How many FDA actions has Abbott Diagnostics Scarborough, Inc. had?: Argus HQ has recorded 7 FDA events for Abbott Diagnostics Scarborough, Inc.: 0 warning letters, 7 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 Diagnostics Scarborough, Inc.?: The most recent FDA event Argus HQ has on file for Abbott Diagnostics Scarborough, Inc. is dated 2026-03-25, with a severity rating of "high" 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.
Does Argus HQ track new FDA actions for Abbott Diagnostics Scarborough, Inc. automatically?: Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Abbott Diagnostics Scarborough, Inc. is observed, this page's event count and history update automatically.
How many FDA actions does Argus HQ track for Abbott Diagnostics Scarborough, Inc.?: 7 total: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.

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

Verified from FDA.gov · Last updated: Mar 25, 2026

Cite this record

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

APA

Argus HQ Research (2026). Regulatory Record: Abbott Diagnostics Scarborough, Inc.. Digital Empire LLC. Retrieved from https://argushq.ai/company/abbott-diagnostics-scarborough-inc

MLA

"Regulatory Record: Abbott Diagnostics Scarborough, Inc.." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/company/abbott-diagnostics-scarborough-inc.

Chicago

Argus HQ Research. "Regulatory Record: Abbott Diagnostics Scarborough, Inc.." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/company/abbott-diagnostics-scarborough-inc.

BibTeX

@misc{argushq_argushq_ai_company_abbott_diagnostics_scarborough_inc_2026,
  title = {Regulatory Record: Abbott Diagnostics Scarborough, Inc.},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/company/abbott-diagnostics-scarborough-inc},
  note = {Accessed: July 17, 2026}
}

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