Angiography/angioplasty Kit
Cardiovascular · 21 CFR 870.1650
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
494 adverse event reports on file
- MERIT CUSTOM KITJul 10, 2026MalfunctionMerit Medical Systems Inc.1721504-2026-00234
- ANGIOGRAPHY PACKJun 11, 2026OtherMedline Industries, Lp - LaredoMW5189356
- ANGIOGRAPHY PACKJun 10, 2026MalfunctionMedline Industries, Lp - LaredoMW5189218
- CUSTOM KITJun 3, 2026MalfunctionMerit Medical Systems, Inc.1721504-2026-00098
- CUSTOM KITMay 22, 2026MalfunctionMerit Medical Systems Inc.1721504-2026-00072
- CUSTOM KITMay 8, 2026MalfunctionMerit Medical Systems, Inc.1721504-2026-00032
- MERIT MEDICAL®May 7, 2026MalfunctionMerit Medical Systems, Inc.25111156
- CUSTOM KITMay 6, 2026MalfunctionMerit Medical Systems, Inc.1721504-2026-00045
- CUSTOM KITApr 17, 2026MalfunctionMerit Medical Systems, Inc.1721504-2026-00015
- CUSTOM KITApr 17, 2026MalfunctionMerit Medical Systems, Inc.1721504-2026-00016
Event type breakdown
Recalls
89 recall events for this product code
- Windstone Medical Packaging, Inc.Open, ClassifiedJul 27, 2026
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio Pack - RX, Part Number AMS9461
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier quality issues.
Z-2815-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJun 25, 2026
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Z-2581-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJun 25, 2026
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Z-2591-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJun 17, 2026
MEDLINE Medical Procedure Kits labeled as: LAPAROSCOPY COMBINED - NO NDL, Medline Kit Number/SKU DYNJ37378A
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
Z-2485-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedMay 8, 2026
Medline medical convenience kits, containing Namic Manifold, Labeled as:
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Z-2143-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedMay 7, 2026
Medline Convenience Kits:
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Z-2091-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedApr 30, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: ANGIO PACK-LF, Medline Kit Number/SKU DYNJ0774765U
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-2014-2026 · View FDA record ↗ - Merit Medical Systems, Inc.Open, ClassifiedApr 29, 2026
Philips Bridge Prep Kit
catheter may experience resistance when being advanced over the guidewire
Z-2002-2026 · View FDA record ↗ - Merit Medical Systems, Inc.Open, ClassifiedApr 29, 2026
Philips Bridge Prep Kit
catheter may experience resistance when being advanced over the guidewire
Z-2003-2026 · View FDA record ↗ - Merit Medical Systems, Inc.Open, ClassifiedApr 29, 2026
Philips Bridge Prep Kit
catheter may experience resistance when being advanced over the guidewire
Z-2004-2026 · View FDA record ↗
Registered firms
55 firms currently registered for this product code
Medical Action Industries, Inc. 306
ARDEN, NC, US
Sterigenics U.s., Llc
Queensbury, NY, US
Sterigenics U.s., Llc
Salt Lake City, UT, US
Merit Medical Australia Pty Ltd.
Braiside Victoria, AU
Tri-state De Mexico, S. De R.l. De C.v.
MEXICALI Baja California, MX
Merit Medical Systems, Inc
Chester, VA, US
Nuevo Laredo Directo Al Cliente
Nuevo Laredo Tamaulipas, MX
Merit Medical Ireland, Ltd
Galway, IE
Global Resources (vietnam) Group Limited Company
Hai Phong City, VN
Medline Industries, Lp - Spt
Waukegan, IL, US
Gri Medical & Electronic Technology Co., Ltd.
JIAXING Zhejiang, CN
Deroyal Industries, Inc.
POWELL, TN, US
Sterigenics U.s., Llc
Ontario, CA, US
Allwell Medical Corporation
Raleigh, NC, US
Merit Medical Systems, Inc.
South Jordan, UT, US
Sterigenics U.s., Llc
Atlanta, GA, US
Medline Canada
Guelph Ontario, CA
Medline Soluciones Medicas
Nuevo Laredo Tamaulipas, MX
Deroyal Industries, Inc.
NEW TAZEWELL, TN, US
Remington Medical, Inc.
ALPHARETTA, GA, US
Medline Industries (namic Division) - Glen Falls
Glens Falls, NY, US
Isomedix Operations Inc
El Paso, TX, US
Merit Medical Canada Ltd.
Markham Ontario, CA
Merit Medical Uk Limited
Earley Reading, GB
Merit Medical Nederland Bv
Maastricht Airport Limburg, NL
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.