Has Stryker Sustainability Solutions had other FDA enforcement actions?

Yes. 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.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2023-05-24; Argus observed and indexed it on 2026-07-16.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Stryker Sustainability Solutions — Class II recall: REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-…

Name: FDA Recall Record — Stryker Sustainability Solutions
Creator: Argus HQ
Published: 2023-05-24
License: https://argushq.ai/methodology

Event date: 2023-05-24 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-1612-2023
Payload hash: af96e077d5e296f478ffe4c8…

Summary

Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be mislabeled and/or mispackaged. Status: Ongoing.

Entities

Stryker Sustainability Solutions

View source record ↗

Frequently asked questions

Has Stryker Sustainability Solutions had other FDA enforcement actions?: Yes. 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.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2023-05-24; Argus observed and indexed it on 2026-07-16.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

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 (2023). Stryker Sustainability Solutions — Class II recall: REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-stryker-sustainability-solutions-z-1612-2023

MLA

"Stryker Sustainability Solutions — Class II recall: REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-…." Argus HQ Research, Digital Empire Holdings LLC, 2023, argushq.ai/events/fda-recall-stryker-sustainability-solutions-z-1612-2023.

Chicago

Argus HQ Research. "Stryker Sustainability Solutions — Class II recall: REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-stryker-sustainability-solutions-z-1612-2023.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_stryker_sustainability_solutions_z_1612_2023_2023,
  title = {Stryker Sustainability Solutions — Class II recall: REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-…},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-stryker-sustainability-solutions-z-1612-2023},
  note = {Accessed: July 23, 2026}
}

Informational only. Not legal, financial, or medical advice.