Has Stryker Sustainability Solutions had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 34 total FDA actions tied to Stryker Sustainability Solutions, including 34 recalls and 0 warning letters.

What is the current status of this recall?

Status as recorded by FDA: Ongoing.

Where can I verify this recall directly with FDA?

The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

FDA Recall Database: Class II Recall: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick… by Stryker Sustainability Solutions

Here's the summary: Stryker Sustainability Solutions recalled Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (additional items listed in FDA's full record) on 2026-04-15. FDA classified this action as a Class II recall (recall number Z-1804-2026). Reason for recall: Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.. Recall status: Ongoing. This is a device-category FDA recall record.

Key facts

Recalling firm	Stryker Sustainability Solutions
Manufacturer	Not disclosed in the FDA record.
Brand name	Not disclosed in the FDA record.
Product description	Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (Red) Dual Port Single Bladder REF 5921-018-235.
Classification	Class II
Recall number	Z-1804-2026
Report date	Not disclosed in the FDA record.
Status	Ongoing
Reason for recall	Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (additional items listed in FDA's full record) -- and the recall number Z-1804-2026. If it matches, stop using or distributing it and contact Stryker Sustainability Solutions or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice.

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Stryker Sustainability Solutions and the affected product is described in FDA's record as: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (additional items listed in FDA's full record). FDA's stated reason for the recall is: Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.. The recall is tracked under FDA recall number Z-1804-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do.

Stryker Sustainability Solutions’s FDA history

Argus HQ has recorded 34 total FDA actions tied to Stryker Sustainability Solutions: 0 warning letters, 34 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Has Stryker Sustainability Solutions had other FDA recalls or enforcement actions?: Yes. Argus HQ has recorded 34 total FDA actions tied to Stryker Sustainability Solutions, including 34 recalls and 0 warning letters.
What is the FDA recall number for this event?: FDA recall number Z-1804-2026.
What is the current status of this recall?: Status as recorded by FDA: Ongoing.
Where can I verify this recall directly with FDA?: The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

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Full FDA history for Stryker Sustainability Solutions

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

Cite this record

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

APA

Argus HQ Research (2026). FDA Recall Database: Class II Recall: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick… by Stryker Sustainability Solutions. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/recall/fda-recall-stryker-sustainability-solutions-z-1804-2026

MLA

"FDA Recall Database: Class II Recall: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick… by Stryker Sustainability Solutions." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/recall/fda-recall-stryker-sustainability-solutions-z-1804-2026.

Chicago

Argus HQ Research. "FDA Recall Database: Class II Recall: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick… by Stryker Sustainability Solutions." Digital Empire Holdings LLC. Accessed July 24, 2026. https://argushq.ai/recall/fda-recall-stryker-sustainability-solutions-z-1804-2026.

BibTeX

@misc{argushq_argushq_ai_recall_fda_recall_stryker_sustainability_solutions_z_1804_2026_2026,
  title = {FDA Recall Database: Class II Recall: Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick… by Stryker Sustainability Solutions},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/recall/fda-recall-stryker-sustainability-solutions-z-1804-2026},
  note = {Accessed: July 24, 2026}
}

Source: FDA.gov — Recalls ↗