O&M HALYARD INC
7 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm. recall (Z-2230-2026) | O&M HALYARD INC | 2026-05-22 |
| Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2 recall (Z-2520-2025) | O&M HALYARD INC | 2025-09-04 |
| Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Ver recall (Z-0983-2025) | O&M HALYARD, INC. | 2025-01-17 |
| O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product recall (Z-0728-2025) | O&M HALYARD, INC. | 2024-12-20 |
| O&M Halyard SOFT TOUCH II Surgical Mask, Blue-Disposable surgical mask Product Code: 47500 recall (Z-0729-2025) | O&M HALYARD, INC. | 2024-12-20 |
| HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100) recall (Z-1461-2024) | O&M HALYARD, INC. | 2024-04-02 |
| FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with SO SOFT* Lining, Or recall (Z-2626-2023) | O&M HALYARD, INC. | 2023-09-21 |
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Every clearance here is in the API, with alerts when new ones post.