Home › Device types › JOL
Catheter And Tip, Suction
FDA product code JOL · Class 2 · General Hospital
6,008
Registered devices
2,832
Adverse events
16
Recalls
84
510(k) clearances
Devices with this code
PRINCETON — Princeton Medical Group, Inc.ESI — FTT MEDICAL, INC.Integra® Ruggles®-Redmond™ — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSymmetry FRAZIER — ASPEN SURGICAL PRODUCTS, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV-Tip — BIO-LIFE INNOVATIONS, LLCAvalign — Avalign Technologies, Inc.SONTEC NEURO SUCTION — SONTEC INSTRUMENTS, INC.AESCULAP — AESCULAP, INC.Integra® Ruggles®-Redmond™ — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAvalign — Avalign Technologies, Inc.Surtex — SURTEX INSTRUMENTS LTD.Millennium — Avalign Technologies, Inc.Millennium — Avalign Technologies, Inc.ESI — FTT MEDICAL, INC.Integra® Ruggles®-Redmond™ — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPROVIEW — Orthofix US LLCHayden Medical — Hayden Medical, Inc.Surtex — SURTEX INSTRUMENTS LTD.Sage Self Oral Care — SAGE PRODUCTS, LLCSurtex — SURTEX INSTRUMENTS LTD.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.Symmetry Surgical RHOTON — ASPEN SURGICAL PRODUCTS, INC.AVANOS — Avanos Medical, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-03-05 | Cook Incorporated | Products from the affected device lots were labeled with expiration dates that exceed the true shelf life. |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster |
| 2024-06-11 | Merit Medical Systems, Inc. | 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 |
| 2023-12-04 | Cardinal Health 200, LLC | Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist. |
| 2023-11-15 | MEDLINE INDUSTRIES, LP - Northfield | Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irr |
| 2023-05-18 | MEDLINE INDUSTRIES, LP - Northfield | Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams. |
| 2019-09-17 | Cook Inc. | Lidstock perforation line may be over the sterile area of the tray, when it should be on the lip of the tray, potentially compromising the sterility of the devi |
| 2019-06-10 | Santanello Surgical LLC | Lack of package integrity may compromise sterility |
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