338 results
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26ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. MAJOR BASIN SET DYNJ85723
FDA Recall
Open, Classified
·Product code KDD·February 27, 2026
DeRoyal Lap Chole Tray, REF 89-4823.06, Rx, Sterile EO. (custom surgical kit)
FDA Recall
Terminated
·DeRoyal Industries Inc·Product code KDD·October 1, 2008
"***REF: 24-4050 TMJ SYSTEM ArthroSimplicity KIT***STERILE PRODUCT***STERILE EO***KIT CONTAINS BOTH STERILE AND NON-STERILE COMPONENTS DISTRIBUTED BY: BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com***" Kit Contains: Drape with pouch; 18Gx1.5in needle; OR towel; Towel clips; Skin marker with ruler; Band-aids; Cotton ball; 5ml syringe; Gauze sponges; Extension tubing; Cholarprep swabsticks; Utility Bowl. All-inclusive kit that alleviates the burden of piecing together each of the items necessary for a Arthroscopy using the OnPoint Scope.
FDA Recall
Terminated
·Biomet Microfixation, Inc.·Product code KDD·October 8, 2010
"***REF: 922070 TMJ SYSTEM ARTHROSIMPLICITY KIT***STERILE PRODUCT***STERILE EO***DISTRIBUTED BY BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com***" THIS KIT WAS DISCONTINUED. Kit Contained: Drape with pouch; 18Gx1.5in needle; OR towel; Towel clips; Skin marker with ruler; Band-aids; Cotton ball; 5ml syringe; 60ml syringe; Gauze sponges; Extension tubing; Chloraprep swabsticks; Utility Bowl. All-inclusive kit that alleviates the burden of piecing together each of the items necessary for a TMJ arthrocentesis procedure.
FDA Recall
Terminated
·Biomet Microfixation, Inc.·Product code KDD·October 8, 2010
BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)
FDA Recall
Open, Classified
·Synergetics Inc·Product code KDD·June 12, 2024
Custom surgical kits labeled as follows: (a) Suture Removal Set, 910-0002 (b) Instrument Set, INST03/20 (c) Suture Removal Set, SUT309/100 (d) Incision & Drainage Tray, INC03/20 (e) Suture Removal Set, SUT103/50 (f) General Purpose Tray, GPT010/25 (g) General Purpose Tray, GPT002/50
FDA Recall
Completed
·Bioseal Corporation·Product code KDD·October 18, 2017
ArrowClarke" PleuraSeal Thoracentesis Kit
FDA Recall
Terminated
·Arrow International Inc·Product code KDD·October 24, 2017
Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS L & D TRAY, Reorder Number MNS9065
FDA Recall
Open, Classified
·MEDLINE INDUSTRIES, LP Northfield·Product code KDD·December 7, 2022
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584003;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001380;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001635;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000759;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001878;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000479;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001417;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000781;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000305;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001423;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000477;
FDA Recall
Open, Classified
·Beaver Visitec International, Inc.·Product code KDD·July 26, 2024