Recall archive
25 recalls · page 1 of 2
Reported Sep 2, 2026Updated Sep 7, 2026
CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product · Product details — Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product · Product details — Potential for overpressure alerts.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unimax Medical Systems Inc.
Matched: Product details — The tube may fall into the surgical site during the grasping process.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction…
FDA (openFDA device enforcement)
Reported May 5, 2021
INFINITY_TRAY Custom Procedural Kit - Canada. containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE100…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Infinity ACL Tibial Elbow Guide-indicated for use in open and arthroscopic procedures for knee ligament reconstruction.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
Matched: Brand · Product · Product details — Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, REF/Catalog Number 2602 Indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 20, 2017
Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Manufactured with the incorrect anchor outer body
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product details — For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons were packaged in error by the manufacturer with non-sterile P/N 7-796-19…
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution Bags, Catalog Number CD8185 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Reason for recall — CONMED received complaints of damage to the CS-023 electrodes shaft insulation which could result in burn marks on the shaft. If the shaft…
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
Matched: Brand — A version of the dual dispersive electrodes may not be compatible with some electrosurgical generators, placing patients at risk for undetected pad…
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Hip Preservation System Signature Series PreBent Burs under the following labels: 1) PreBent Spherical Bur, 5.5mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product details — Metal shavings released from burs during use are due to contact between the bur and the hood of the PreBent Bur assembly. During the manufacturing…
FDA (openFDA device enforcement)
Reported Dec 9, 2015
Altrus Thermal Tissue Fusion Energy Sources, Catalog Numbers: 1) 60-9500-120 & 2) 60-9500-INT. Thermal Ligation and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Miscalibration of the Energy Source monitoring function, which may incorrectly sense the handpiece temperature as higher than the actual handpiece's…
FDA (openFDA device enforcement)
Reported Nov 11, 2015
Arthroscopic Energy 50¿ Probe with Suction, Catalog number: AES-50S Peoduct Usage: For resection, ablation, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand — Probe programming error. The incorrect program can generate more heat at the surgical site, resulting in an elevated probability of tissue damage.
FDA (openFDA device enforcement)
Reported Dec 10, 2014
ADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ConMed Corporation
Matched: Brand — Philips Healthcare made changes to the design of the connection between multifunction electrodes and their HeartStart FR3 and HeartStart FRx AEDs.…
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2014
Altrus Thermal Tissue Fusion Handpieces under the following specifications: 1) 10mm x 16 cm Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Reason for recall — ConMed Corporation initiated an Urgent Medical Device Correction for Altrus Thermal Tissue Fusion Handpieces due to risk of burns.
FDA (openFDA device enforcement)
Reported Jun 11, 2014
MACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. The device is applied to the patient during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product · Product details · Reason for recall — ConMed Corporation has received complaints regarding sparking, no output and burning at the cord set connection. The complaints have been confirmed…
FDA (openFDA device enforcement)
Reported Nov 27, 2013
ALTRUS¿ THERMAL TISSUE FUSION, Tissue Fusion Handpiece, 5 mm O.D., 16 cm Shaft, REF 60-9520-001, STERILE -- CONMED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product · Product details · Reason for recall — The affected lots were exposed to a higher than acceptable level of particulate matter during manufacture and subsequently distributed. ConMed…
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2013
PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C. The PadPro(R) Adult…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Reason for recall — ConMed was notified by the contract manufacturer that their wire/connector supplier reported damage to the connector tooling which could pinch or…
FDA (openFDA device enforcement)
Reported Feb 27, 2013
ELECTROLASE HYFRECATOR(R) ELECTRODES - SHARP, REF/Catalog Number 7-100-8BX, Disposable Hyfrecator(R) Tips, Sterile, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product details · Reason for recall — Some devices had broken through the seal of the sterile pouch. ConMed confirmed instances where the pouch seal was compromised on the affected…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2013
ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP, Disposable Hyfrecator(R) Tips, REF/Catalog No. 7-100-8CS, Sterile, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
Matched: Brand · Product details · Reason for recall — ConMed received complaints of some devices which had broken through the seal of the sterile pouch. ConMed confirmed instances where the pouch seal…
19 more products in this recall
FDA (openFDA device enforcement)
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