54 results
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29ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 102004-000050 c) I.D. mm 6,0, Product Code 102004-000060 d) I.D. mm 7,0, Product Code 102004-000070 e) I.D. mm 8,0, Product Code 102004-000080 Product Usage: Tracheal intubation during laser surgery in the laryngeal area. The tube is resistant to the following kinds of laser: A R+ laser / ND/YAG laser / CO2 lasers (continuous-wave or pulsed) with a wave length ranging from 0.488 m to 10.6 m.
FDA Recall
Terminated
·TELEFLEX MEDICAL INC·Product code BTR·May 29, 2020
Restoration Hip system Cylindrical Distal Extension. Catalog Numbers 1212-3105, 1212-3115, 1212-3125, and 1212-3195. Sizes 12.5mm, 11.5mm, 19.5mm, and 10.5mm extensions.
FDA Recall
Terminated
·Stryker Howmedica Osteonics·Product code LXH·February 10, 2004
RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0
FDA Recall
Terminated
·Teleflex Medical·Product code BTR·April 1, 2019
RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0
FDA Recall
Terminated
·Teleflex Medical·Product code BTR·April 1, 2019
RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0
FDA Recall
Terminated
·Teleflex Medical·Product code BTR·April 1, 2019
RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0
FDA Recall
Terminated
·Teleflex Medical·Product code BTR·April 1, 2019
RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0
FDA Recall
Terminated
·Teleflex Medical·Product code BTR·April 1, 2019
Radionics Head and Neck Localilizer (HNL), Version B
FDA Recall
Terminated
·Radionics, Inc.·Product code MUJ·May 25, 2004
Alsius CoolGard 3000 patient temperature regulation system
FDA Recall
Terminated
·Alsius Corporation·Product code NCX·November 10, 2004
Biolox Ceramic Head XL
FDA Recall
Terminated
·Plus Orthopedics·Product code LZO·February 10, 2004
Optima Spinal System and Spinal Hook System, set screw component.
FDA Recall
Terminated
·U & I America·Product code MNI·August 10, 2004
VerifyNow Asprin Assay Kit Part No. 85034
FDA Recall
Terminated
·Accumetrics Inc·Product code JOZ·May 10, 2004
Foundation Knee System, Tibia-Nonporous, Size 6, Right, sterile. Manufactured by Encore Orthopeadics, 9800 Metric Blvd., Austin, Texas 78758
FDA Recall
Terminated
·Product code JWH·May 10, 2004
Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.
FDA Recall
Terminated
·Stryker Medical·Product code FPO·August 17, 2004
3DKnee System, Stemmed Tibia-Nonporous-3D, Size 6, Right, sterile. Manufactured by Encore Orthopeadics, 9800 Metric Blvd., Austin, Texas 78758
FDA Recall
Terminated
·Product code JWH·May 10, 2004
Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025
Allura Xper CV20; Model Numbers: 722031; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025
Power Heart AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9142
FDA Recall
Terminated
·Cardiac Science, Inc.·Product code MKJ·May 4, 2004
FirstSave AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9143
FDA Recall
Terminated
·Cardiac Science, Inc.·Product code MKJ·May 4, 2004
Allura Xper FD20/20; Model Numbers: 722038; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025