company
O&M HALYARD INC
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-03O&M HALYARD INC — Class II recall: Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS),…
Frequently asked questions
- How many FDA warning letters has O&M HALYARD INC received?
- Argus HQ has not recorded an FDA warning letter for O&M HALYARD INC in our current dataset.
- What FDA recalls has O&M HALYARD INC issued?
- Argus HQ has recorded 1 FDA recall tied to O&M HALYARD INC.
- Is O&M HALYARD INC FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for O&M HALYARD INC. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.

