125 results · 28ms · Sources: EU EUDAMED, US FDA

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Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box, each catheter is packaged in an individual pouch. Urinary catheter.

FDA Recall
Terminated ·C.R. Bard, Inc.·Product code EZD·September 14, 2017

Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818

FDA Recall
Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

LoFric Origo, Tiemann, 16in, FR14 urinary catheters

FDA Recall
Terminated ·Wellspect HealthCare (Division of DENTSPLY IH AB) Aminogatan 1 Molndal Sweden·Product code EZD·June 17, 2020

HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818

FDA Recall
Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G

FDA Recall
Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

Male, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in intermediate boxes containing 30 individual, sterile packaged catheters (PA/PE film and dialyzing paper pouches). There are 30 catheters packaged in sterile pouches that are placed into an intermediate box, 10 of these intermediate boxes packaged into one case. K072539 The Cure Catheter" device, M16, is an intermittent urinary catheter intended to be used by males for the purpose of bladder drainage. It is manufactured with conventional medical grade, latex-free, biocompatible materials. The straight-tip has been designed to eliminate trauma to the urethra and is provided in 16Fr size in an easy-to-open, sterile, single-use package. The coud-tip catheter, M16C, is designed with a curved tip that makes it easier to pass through the curvature of the prostatic urethra in men. It is also used to pass through urethral strictures. This product is prescribed for people who have difficulty or are unable to pass a straight catheter through their urethra and into their bladder.

FDA Recall
Terminated ·Cure Medical LLC·Product code EZD·September 19, 2012

Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch, Item Numbers: 50612, 50614, 50616, 50618, 52306, 52308, 52310, 52606, 52606G, 52608, 52608G, 52610, 52610G, 53314, 53320, 53514G, 53610, 53610G, 53612G, 53614G, 53616G, 53618G, 62308, 62310, 62606P, 602608, 62608P, 62610, 62610P, 63310, 63316, 63610, 63610M, 63612, 63612M, 63614, 63614M, 63616, 63616M, 63618, 71410, 72608, 72610, 73612, 73614, 73616 Product Usage Intermittent catheters are intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.

FDA Recall
Terminated ·C.R. Bard, Inc.·Product code EZD·September 14, 2017

Pediatric, 10Fr, Intermittent Urinary Catheters Model: P10 Pouch Label UPC (P10) *+M405P100C* Intermediate Box Label UPC (P10) *+M405P103F* Carton Label UPC (P10) *+M405P105H* The product is distributed individually or in intermediate boxes containing 30 individual, sterile packaged catheters (PA/PE film and dialyzing paper pouches). There are 30 catheters packaged in sterile pouches that are placed into an intermediate box, 10 of these intermediate boxes packaged into one case. Intended to be used by pediatric males and females for the purpose of bladder drainage

FDA Recall
Terminated ·Cure Medical LLC·Product code EZD·November 11, 2014

LoFric Origo, Tiemann, 16in, FR12 urinary catheters

FDA Recall
Terminated ·Wellspect HealthCare (Division of DENTSPLY IH AB) Aminogatan 1 Molndal Sweden·Product code EZD·June 17, 2020

HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch. MGC3 Product Usage Intermittent catheters are intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.

FDA Recall
Terminated ·C.R. Bard, Inc.·Product code EZD·September 14, 2017

LoFric Origo, Nelaton, 16in, FR10 urinary catheters

FDA Recall
Terminated ·Wellspect HealthCare (Division of DENTSPLY IH AB) Aminogatan 1 Molndal Sweden·Product code EZD·June 17, 2020

SureCath Set with Accessories, Coloplast Corp.-MN 06093, Sterile EO., Manufacturer Coloplast -A/S 3050 Denmark. 28022S 1400 SureCath Set,acc CH8 Male,bulk 28023S 1400 Surecath Set,acc CH10 Male,bul 28024S 1400 Surecath Set,acc CH12 Male,bul 280320 1400 SureCath Set,acc CH14 Male 28032S 1400 Surecath Set,acc CH14 Male,bul 28036S 1400 Surecath Set,acc CH14/1,2 Male 28037S 1400 Surecath Set,acc CH16 Male 280370 1400 Surecath Set,acc CH16 Male 28033S 1400 Surecath Set,acc CH16 Male 280360 1400 Surecath Set,acc CH14/1,2 Male 280340 1400 SURECATH SET W.ACC FEM14` The SureCath Set is indicated for use by patients for intermittent catherization for the purpose of bladder drainage. The insertion supplies provided are to be used to insert the catheter using sterile technique.

FDA Recall
Terminated ·Coloplast Manufacturing US, LLC·Product code EZD·April 21, 2011

Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF 50816G, e) REF 50818G, f) REF 53810G, g) REF 53812G, h) REF 53814G, i) REF 53816G, j) REF 53818G, k) REF 53820G

FDA Recall
Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

VisuaLine Tricyclic Antidepressants: Six Dip (COC-THC-OPI-MET-BZD-OXD); Six Dip (COC-THC-OPI-MET-PCP-OXD); Eight DIP (COC-THC-OPI-MET-AMP-BAR-BZD-OXD); Nine Dip (COC-THC-OPI-MET-PCP-AMP-BAR-BZD-TCA); Ten Dip X (COC-THC-OPI-MET-PCP-AMP-BAR-BZD-MTD-TCA); Ten Dip (COC-THC-OPI-MET-PCP-AMP-BAR-BZD-MTD-OXD); Ten Dip (COC-THC-OPI-MET-PCP-AMP-BAR-BZD-TCA-OXD); Five Dip (COC-THC-OPI-BZD-OXD); and Six Dip (CPC-THC-OPI-MET-AMP-OXD). Product is intended for in vitro immunoassay test completed by visual color comparison used for the detection of drugs of abuse.

FDA Recall
Terminated ·Sun Biomedical Laboratories, Inc.·Product code DJR·May 28, 2008

DrugCheck 8 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP Product Code 60800

FDA Recall
Terminated ·Drug Free Enterprises Inc·Product code DIO·March 20, 2003

DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/TCA Product Code 60900

FDA Recall
Terminated ·Drug Free Enterprises Inc·Product code DIO·March 20, 2003

DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/MTD Product Code 60925

FDA Recall
Terminated ·Drug Free Enterprises Inc·Product code DIO·March 20, 2003

Toshiba America Medical Systems, Ultimax System MDX-8000A equipped with the EPS-Plus/ADR-1000A/E2D Digital Spot Film Device

FDA Recall
Terminated ·Toshiba American Med Sys Inc·Product code LLZ·February 23, 2006

Hudson RCI One Way Valve, 22mm E.D. to 22mm O.D., REF 1665, Rx Only, Teleflex Medical, Research Triangle park, NC 27709

FDA Recall
Terminated ·Telefelx Medical·Product code BZA·December 2, 2009

Harleco May and Grunwald's Stain; 0.17% w/v; Methanol Solution UN1230; EMD Chemicals Inc. An Affilifate of Merck KGaA Damstadt, Germany; 480 South Democrat Road; Gibbstown, NJ 08027; 1 liter and 4 liter poly bottles

FDA Recall
Terminated ·EMD Chemicals Inc·Product code KQC·July 30, 2007