Zimmer Surgical Inc — FDA Enforcement History

FDA action counts

Enforcement history

On 2026-07-08, Argus HQ recorded an FDA recall for Zimmer Surgical Inc, rated "high" severity in Argus HQ's classification: Zimmer Surgical Inc — Class II recall: Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Sy…. On 2026-07-08, Argus HQ recorded an FDA recall for Zimmer Surgical Inc, rated "high" severity in Argus HQ's classification: Zimmer Surgical Inc — Class II recall: Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Sy…. 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.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Zimmer Surgical Inc has 2 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

Is this FDA enforcement data for Zimmer Surgical Inc 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 Zimmer Surgical Inc had?

Argus HQ has recorded 2 FDA events for Zimmer Surgical Inc: 0 warning letters, 2 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 Zimmer Surgical Inc?

The most recent FDA event Argus HQ has on file for Zimmer Surgical Inc is dated 2026-07-08, 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 Zimmer Surgical 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 Zimmer Surgical Inc is observed, this page's event count and history update automatically.

Related enforcement actions

• Zimmer Surgical Inc — Class II recall: Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Sy… →
• Zimmer Surgical Inc — Class II recall: Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Sy… →
• Zimmer Surgical Inc — Class II recall: Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet S… →
• Zimmer Surgical Inc — Class II recall: Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet S… →
• Zimmer Surgical Inc — Class II recall: Zimmer Air Dermatome, Model/Catalog Number: 00880100100 →
• Zimmer Surgical Inc — Class II recall: Zimmer Dermatome AN, Model/Catalog Number: 88710100 →
• Zimmer Surgical Inc — Class II recall: 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier →
• Zimmer Surgical Inc — Class II recall: Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the derm… →

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