ConMed Corporation recalls

40 recalls on record · latest: November 18, 2022

Official U.S. recall history for ConMed Corporation, compiled from official government records.

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ConMed Corporation recalls Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187

November 18, 2022 · Medical device recalls Moderate risk Suction ports may potentially be occluded on the affected devices. If this occu…

ConMed Corporation recalls KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE1…

March 26, 2021 · Medical device recalls Moderate risk Tip Guides are potentially misaligned laterally which could affect the accuracy…

ConMed Corporation recalls INFINITY_TRAY Custom Procedural Kit - Canada. containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE100…

March 26, 2021 · Medical device recalls Moderate risk Tip Guides are potentially misaligned laterally which could affect the accuracy…

ConMed Corporation recalls Infinity ACL Tibial Tip Guide- indicated for use in open and arthroscopic procedures for knee ligament reconstruction.…

November 12, 2020 · Medical device recalls Moderate risk Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned…

ConMed Corporation recalls Infinity ACL Tibial Elbow Guide-indicated for use in open and arthroscopic procedures for knee ligament reconstruction.…

November 12, 2020 · Medical device recalls Moderate risk Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned…

Conmed Corporation recalls ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval Syste…

March 21, 2019 · Medical device recalls Moderate risk Voids in the seal or a partial seal results in an open channel and may compromi…

Conmed Corporation recalls ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 The Anchor Tissue Retrieval Syste…

March 21, 2019 · Medical device recalls Moderate risk Voids in the seal or a partial seal results in an open channel and may compromi…

Conmed Corporation recalls ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 The Anchor Tissue Retrie…

March 21, 2019 · Medical device recalls Moderate risk Voids in the seal or a partial seal results in an open channel and may compromi…

Conmed Corporation recalls ConMed Anchor Tissue Retrieval System, 15 MM, 1850 ML (3/BX) Catalog Number:TRS190SB2 The Anchor Tissue Retrieval Syste…

March 21, 2019 · Medical device recalls Moderate risk Voids in the seal or a partial seal results in an open channel and may compromi…

Conmed Corporation recalls ConMed Anchor Tissue Retrieval System, 8 MM, 125 ML (5/BX) Catalog Number:TRS-ROBO-8 The Anchor Tissue Retrieval System…

March 21, 2019 · Medical device recalls Moderate risk Voids in the seal or a partial seal results in an open channel and may compromi…

Conmed Corporation recalls ConMed Anchor Tissue Retrieval System", 12 MM, 300 ML (5/BX) Catalog Number: TRS-ROBO-12 The Anchor Tissue Retrieval Sy…

March 21, 2019 · Medical device recalls Moderate risk Voids in the seal or a partial seal results in an open channel and may compromi…

MINI INFANT < recalled over sterility concerns

February 23, 2018 · Medical device recalls Moderate risk Wire sets of certain devices were assembled with adhesive on the contact wires,…

MINI INFANT < recalled over sterility concerns

February 23, 2018 · Medical device recalls Moderate risk Wire sets of certain devices were assembled with adhesive on the contact wires,…

MINI INFANT < recalled over sterility concerns

February 23, 2018 · Medical device recalls Moderate risk Wire sets of certain devices were assembled with adhesive on the contact wires,…

MINI INFANT < recalled over sterility concerns

February 23, 2018 · Medical device recalls Moderate risk Wire sets of certain devices were assembled with adhesive on the contact wires,…

MINI INFANT < recalled over sterility concerns

February 23, 2018 · Medical device recalls Moderate risk Wire sets of certain devices were assembled with adhesive on the contact wires,…

ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog Num…

June 19, 2017 · Medical device recalls Moderate risk Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inc…

ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets and Extension Sets (Catalog Numbers: (1) S…

June 19, 2017 · Medical device recalls Moderate risk Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inc…

ConMed Corporation recalls Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be us…

April 17, 2017 · Medical device recalls Moderate risk Manufactured with the incorrect anchor outer body

HYFRECATOR 2000 HANDPIECE SHEATH recalled over sterility concerns

February 28, 2017 · Medical device recalls Moderate risk For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons were…

Sterile Handpiece Sheaths recalled over sterility concerns

February 28, 2017 · Medical device recalls Moderate risk For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons were…

Sterile Handpiece Sheaths recalled over sterility concerns

February 28, 2017 · Medical device recalls Moderate risk For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons were…

Sterile Handpiece Sheaths recalled over sterility concerns

February 28, 2017 · Medical device recalls Moderate risk For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons were…

Sterile Handpiece Sheaths recalled over sterility concerns

February 28, 2017 · Medical device recalls Moderate risk For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons were…

ConMed Corporation recalls CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only Product Usage: The Hea…

August 29, 2016 · Medical device recalls Moderate risk CONMED received complaints of damage to the CS-023 electrodes shaft insulation…