Tracheobronchial Suction Catheter Kit
Anesthesiology · 21 CFR 868.6810
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
Recent MDR events
22 adverse event reports on file
- MEDLINEJul 21, 2026MalfunctionMedline Industries, Lp1417592-2026-07263
- MEDLINEJun 2, 2026MalfunctionMedline Industries, Lp1417592-2026-01996
- MEDLINEJun 1, 2026MalfunctionMedline Industries, Lp1417592-2026-01946
- MEDLINEMay 22, 2026MalfunctionMedline Industries, Lp1417592-2026-01518
- CLEARPRO¿ TRACH T-PIECE CLOSED SUCTION CATHETER, 14 FRENCHMay 5, 2026MalfunctionMedline Industries, Lp1417592-2026-00877
- CLEARPRO¿ TRACH T-PIECE CLOSED SUCTION CATHETER, 14 FRENCHMay 1, 2026MalfunctionMedline Industries, Lp1417592-2026-00787
- MEDLINEApr 9, 2026MalfunctionMedline Industries, Lp1417592-2026-00399
- MEDLINEMar 11, 2026MalfunctionMedline Industries, Lp1417592-2026-00208
- MEDLINEFeb 18, 2026MalfunctionMedline Industries, Lp1417592-2026-00129
- CLEARPRO,CLOSED SXN,14FR,D SWVL,ETTSep 12, 2025InjuryMedline Industries, Lp1417592-2025-00469
Event type breakdown
Recalls
6 recall events for this product code
- Medline Industries, LPOpen, ClassifiedApr 30, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: EH BRONCHOSCOPY, Medline Kit Number/SKU DYNJT3270
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
Z-2010-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedApr 1, 2026
Medline convenience kits containing Olympus biopsy valves:
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
Z-1706-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedFeb 6, 2026
Medline 14 Fr Suction Catheter Kits
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
Z-1312-2026 · View FDA record ↗ - MEDLINE INDUSTRIES, LP - NorthfieldOpen, ClassifiedDec 5, 2024
MEDLINE convenience kits labeled as:
Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
Z-0629-2025 · View FDA record ↗ - MEDLINE INDUSTRIES, LP - NorthfieldOpen, ClassifiedSep 6, 2024
Medline Convenience kits, labeled as:
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Z-2985-2024 · View FDA record ↗ - MEDLINE INDUSTRIES, LP - NorthfieldOpen, ClassifiedFeb 25, 2024
MEDLINE kits and trays, labeled as:
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Z-1092-2024 · View FDA record ↗
Registered firms
31 firms currently registered for this product code
Suzhou Jingle Polymer Medical Apparatus Co., Ltd.
SUZHOU Jiangsu, CN
Principle & Will Biotech (pinghu) Co., Ltd.
Pinghu City Zhejiang, CN
Amsino Medical (kunshan) Co., Ltd.
KUNSHAN CITY Jiangsu, CN
Cardinal Health 200, Llc
Waukegan, IL, US
Dongguan Hong De Medical Plastic Products Co. Ltd.
Dongguan Guangdong, CN
Nuevo Laredo Directo Al Cliente
Nuevo Laredo Tamaulipas, MX
Productos Medline S.a. De C.v.
NUEVO LAREDO Tamaulipas, MX
Isomedix Operations Inc
EL PASO, TX, US
Allmed Industrial Limited
Shenzhen City Guangdong, CN
Teleflex Medical Llc
Morrisville, NC, US
Cardinal Health 200, Llc
El Paso, TX, US
Midwest Sterilization Corp.
LAREDO, TX, US
Centurion Medical Products, Lp
Williamston, MI, US
Convertors De Mexico S. De R.l. De C.v
CD.JUAREZ Chihuahua, MX
Medline Soluciones Medicas
Nuevo Laredo Tamaulipas, MX
Tri-state De Mexico, S. De R.l. De C.v.
MEXICALI Baja California, MX
Sterigenics Shanghai Eto Ltd.
Shanghai, CN
Medline Industries, Lp - Laredo
LAREDO, TX, US
Steris Sterilization Technologies (suzhou) Ltd
Suzhou Jiangsu, CN
Medline Canada
Guelph Ontario, CA
Medline Industries, Lp - Northfield
Northfield, IL, US
Sterigenics Us Llc
Grand Prairie, TX, US
Medline Industries, Lp - Spt
Waukegan, IL, US
Allmed Medical Products Co., Ltd.
ZHIJIANG CITY Hubei, CN
Allmed Medical Products Co., Ltd.
Zhijiang City Hubei, CN
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.