Home › Device types › JCX
Apparatus, Suction, Ward Use, Portable, Ac-Powered
FDA product code JCX · Class 2 · General, Plastic Surgery
208
Registered devices
2,026
Adverse events
24
Recalls
77
510(k) clearances
Devices with this code
UltrafleX Quad — DORNOCH MEDICAL SYSTEMS, INC.Gomco — Allied Medical, LLCNA — STRYKER CORPORATIONRoscoe Medical — COMPASS HEALTH BRANDS CORP.DeVilbiss — Drive Devilbiss HealthcareIntelliCart™ — ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.Neptune 2 — STRYKER CORPORATIONCliq Aspirator — ANEST IWATA SPARMAX Co., Ltd.Cliq Aspirator — ANEST IWATA SPARMAX Co., Ltd.DeVilbiss — DEVILBISS HEALTHCARE LLCDeVilbiss — DEVILBISS HEALTHCARE LLCNA — ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.Neptune — STRYKER CORPORATIONLCSU 4, 800 ml, RTCA Complete Unit — Laerdal Medical ASPortable Suction — SUNSET HEALTHCARE SOLUTIONS, INC.Neptune — STRYKER CORPORATIONNA — ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.Riptide Collection Canister with Intermediate Tubing — Micro Therapeutics, Inc.Closed Suction — SUNSET HEALTHCARE SOLUTIONS, INC.ASEPT — B BRAUN INTERVENTIONAL SYSTEMS, INCIntelliCart™ — ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.DeVilbiss — DEVILBISS HEALTHCARE LLCNA — ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.DeVilbiss — DEVILBISS HEALTHCARE LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-06 | Stryker Corporation | It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing |
| 2026-01-13 | Laerdal Medical Corporation | units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 2 |
| 2020-12-18 | Laerdal Medical (Suzhou) Co., Ltd. | Component failures may cause the unit to lose all suction. Users will need to obtain alternate suction devices or methods, leading to a delay in treatment and, |
| 2017-08-31 | Laerdal Medical Corporation | A shipment of LCSU 4 suction units and canisters attempted importation into the United States but was refused by FDA for lack of necessary approvals with CDRH |
| 2017-01-08 | Laerdal Medical Corporation | The On/Off functionality in the LCSU 4 is controlled by electronic components, one of which might be damaged. |
| 2016-07-01 | Stryker Instruments Div. of Stryker Corporation | Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on 07/01/2016, due to a potential for the device to experience system errors causing the devi |
| 2016-05-23 | DeVilbiss Healthcare LLC | A small percentage of units of 7305 Series Vacu-Aide Suction Units are experiencing premature failure during operation. |
| 2015-06-04 | Gardner Denver Thomas Inc | Vacuum pump may not perform to specification. |
| 2015-06-04 | Gardner Denver Thomas Inc | Vacuum pump may not perform to specification. |
| 2015-06-04 | Gardner Denver Thomas Inc | Vacuum pump may not perform to specification. |
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