FDA action counts
| Total FDA actions | 18 |
|---|---|
| Warning letters | 0 |
| Recalls | 18 |
| Approval records | 0 |
| Form 483 inspection citations | 0 |
| Most recent action | March 25, 2026 |
Risk pattern analysis
Argus HQ analysis — not an FDA finding
This section is Argus HQ analysis, not an FDA finding. Stryker Medical Division of Stryker Corporation has 18 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.
Enforcement history
On 2026-03-25, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: Cub Pediatric Crib, Model FL19H. On 2025-12-17, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: Stryker MV3 bariatric bed, Part Number 5900000001. On 2025-12-17, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: Stryker Arise 1000EX mattress, Part Number 2236000000. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-LEX-400.. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-LEX-450.. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 300900000000,. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-LE-450.. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCurity bed series, model number 3009, item number: 3009PX-ZX-450.. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-L-200. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-L-100.. On 2023-12-13, Argus HQ recorded an FDA recall for Stryker Medical Division of Stryker Corporation, rated "high" severity in Argus HQ's classification: Stryker Medical Division of Stryker Corporation — Class II recall: ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450..
Frequently asked questions
- Has Stryker Medical Division of Stryker Corporation had product recalls?
- Yes, 18 recalls on file. See the full history below for each one.
- Is this FDA enforcement data for Stryker Medical Division of Stryker Corporation 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 Stryker Medical Division of Stryker Corporation had?
- Argus HQ has recorded 18 FDA events for Stryker Medical Division of Stryker Corporation: 0 warning letters, 18 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 Stryker Medical Division of Stryker Corporation?
- The most recent FDA event Argus HQ has on file for Stryker Medical Division of Stryker Corporation 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.
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Related enforcement actions
- Stryker Medical Division of Stryker Corporation — Class II recall: Cub Pediatric Crib, Model FL19H →
- Stryker Medical Division of Stryker Corporation — Class II recall: Stryker Arise 1000EX mattress, Part Number 2236000000 →
- Stryker Medical Division of Stryker Corporation — Class II recall: Stryker MV3 bariatric bed, Part Number 5900000001 →
- Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-Z-450. →
- Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-LE-400. →
- Stryker Medical Division of Stryker Corporation — Class II recall: ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600. →
- Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-ZM-600. →
- Stryker Medical Division of Stryker Corporation — Class II recall: ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450. →
- Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-L-100. →
- Stryker Medical Division of Stryker Corporation — Class II recall: ProCuity bed series, model number 3009, item number: 3009PX-L-200 →
Compare with
- Stryker Medical Division of Stryker Corporation vs Philips North America
- Stryker Medical Division of Stryker Corporation vs Boston Scientific Corporation
- Stryker Medical Division of Stryker Corporation vs Medline Industries, LP
- Stryker Medical Division of Stryker Corporation vs Baxter Healthcare Corporation
- Stryker Medical Division of Stryker Corporation vs PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Two different companies merged onto this page by mistake? Or a name variant missing? Tell us — corrections@argushq.ai
Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Verified from FDA.gov · Last updated: Mar 25, 2026Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). Stryker Medical Division of Stryker Corporation's Complete FDA Record. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/stryker-medical-division-of-stryker-corporation
"Stryker Medical Division of Stryker Corporation's Complete FDA Record." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/stryker-medical-division-of-stryker-corporation.
Argus HQ Research. "Stryker Medical Division of Stryker Corporation's Complete FDA Record." Digital Empire Holdings LLC. Accessed July 17, 2026. https://argushq.ai/company/stryker-medical-division-of-stryker-corporation.
@misc{argushq_argushq_ai_company_stryker_medical_division_of_stryker_corporation_2026,
title = {Stryker Medical Division of Stryker Corporation's Complete FDA Record},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire Holdings LLC},
url = {https://argushq.ai/company/stryker-medical-division-of-stryker-corporation},
note = {Accessed: July 17, 2026}
}Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗

