Home › Device types › OHR
Catheter Care Tray
FDA product code OHR · Class 2 · Gastroenterology, Urology
494
Registered devices
944
Adverse events
16
Recalls
0
510(k) clearances
Devices with this code
Medline — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.CURE MEDICAL — CONVATEC, PURCHASING DEPARTMENTLSL HEALTHCARE — LSL Industries, LLCMedline — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.TruAdvance — HR PHARMACEUTICALS INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.Medline — MEDLINE INDUSTRIES, INC.Geri-Gentle — GERI-GENTLE CORPORATIONMedline — MEDLINE INDUSTRIES, INC.Magic3™ Antibacterial Hydrophilic Intermittent Catheter, Female — Rochester Medical CorporationMedline — MEDLINE INDUSTRIES, INC.Bard® Foley Catheterization Tray — C. R. Bard, Inc.Duette™ — POIESIS MEDICAL, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Magic3™ Antibacterial Hydrophilic Intermittent Catheter, Male — Rochester Medical Corporation
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2026-05-04 | Medline Industries, LP | During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularitie |
| 2025-09-30 | Medline Industries, LP | Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has |
| 2024-10-09 | MEDLINE INDUSTRIES, LP - Northfield | Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker. |
| 2024-09-04 | MEDLINE INDUSTRIES, LP - Northfield | It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee |
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