Gynecological Laparoscopic Kit
Obstetrics/Gynecology · 21 CFR 884.1720
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
330 adverse event reports on file
- MedlineJul 28, 2026MalfunctionMedline Industries, Lp - Spt1423395-2026-00429
- MEDLINEJul 7, 2026MalfunctionMedline - Mexicali1423395-2026-00357
- MEDLINEJun 30, 2026MalfunctionProductos Medline S.a. De C.v.1423395-2026-00330
- MEDLINEJun 19, 2026MalfunctionMedline Industries, Lp - Spt1423395-2026-00301
- MEDLINEJun 17, 2026MalfunctionMedline Industries, Lp - Spt1423395-2026-00288
- MEDLINEMay 11, 2026MalfunctionProductos Medline S.a. De C.v.1423395-2026-00142
- UPSYLON Y MESH KITApr 23, 2026MalfunctionBoston Scientific Corporation2124215-2026-22037
- MEDLINEApr 14, 2026MalfunctionMedline Industries, Lp - Spt1423395-2026-00089
- CARDINAL HEALTHApr 9, 2026MalfunctionCardinal Health 200, Llc24828611
- MEDLINEApr 1, 2026MalfunctionMedline Industries, Lp1423395-2026-00058
Event type breakdown
Product problems
Reported product problem codes, most common first
Trend for “Adverse Event Without Identified Device or Use Problem”
Recalls
52 recall events for this product code
- Medline Industries, LPOpen, ClassifiedJul 23, 2026
Medline convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) 5cc balloons.
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.
Z-2780-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJul 23, 2026
Medline convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) 5cc balloons.
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.
Z-2782-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJul 23, 2026
Medline convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) 5cc balloons.
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.
Z-2783-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJul 23, 2026
Medline convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) 5cc balloons.
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.
Z-2784-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJul 23, 2026
Medline convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) 5cc balloons.
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.
Z-2785-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJul 23, 2026
Medline convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) 5cc balloons.
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.
Z-2786-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJun 17, 2026
MEDLINE Medical Procedure Kits labeled as
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-2503-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedJun 12, 2026
Medline convenience kits:
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Z-2431-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedMay 7, 2026
See full list in RES, exceeds character limit
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-2109-2026 · View FDA record ↗ - Medline Industries, LPOpen, ClassifiedApr 30, 2026
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. SPINE PROCEDURES PACK-LF, Medline Kit Number/SKU DYNJ0751220P;
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-2034-2026 · View FDA record ↗
Registered firms
29 firms currently registered for this product code
Isomedix Operations Inc
El Paso, TX, US
Medline Soluciones Medicas
Nuevo Laredo Tamaulipas, MX
Medical Action Industries, Inc. 306
ARDEN, NC, US
Avid Medical, Inc. A Medical Action Ind. Company 305
TOANO, VA, US
Sterigenics U.s., Llc
Ontario, CA, US
Medline Industries, Lp - Laredo
LAREDO, TX, US
Sterigenics Us Llc
Grand Prairie, TX, US
Gri Medical & Electronic Technology Co., Ltd.
JIAXING Zhejiang, CN
Proxy Biomedical Ltd.
GALWAY, IE
Boston Scientific Corporation
Marlborough, MA, US
Medline Industries, Lp - Spt
Waukegan, IL, US
Convertors De Mexico S. De R.l. De C.v
CD.JUAREZ Chihuahua, MX
Deroyal Industries, Inc.
NEW TAZEWELL, TN, US
Deroyal Industries, Inc.
NEW TAZEWELL, TN, US
Honduras Kitting, S.a.
Villanueva Cortes, HN
Boston Scientific Corporation
Coventry, RI, US
Productos Medline S.a. De C.v.
NUEVO LAREDO Tamaulipas, MX
Deroyal Industries, Inc.
POWELL, TN, US
Cardinal Health 200, Llc
Waukegan, IL, US
Deroyal Industries, Inc.
NEW TAZEWELL, TN, US
Boston Scientific Corporation
Saint Paul, MN, US
Midwest Sterilization Corp.
LAREDO, TX, US
Cardinal Health 200, Llc
El Paso, TX, US
Midwest Sterilization Corp.
JACKSON, MO, US
Sterigenics U.s., Llc
Charlotte, NC, US
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.