ConMed Corporation recalls
Every recall we track for ConMed Corporation — 30 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from ConMed Corporation peaked in 2019 (6); 30 since 2017. 3% rated “stop using now”.
All FDA recall records for ConMed Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 2 | 0 | 2 |
| 2018 | 1 | 2 | 2 | 0 | 5 |
| 2019 | 0 | 0 | 6 | 0 | 6 |
| 2020 | 0 | 0 | 2 | 0 | 2 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 5 | 7 | 0 | 12 |
Most common reasons for ConMed Corporation recalls
What to do if you have a recalled ConMed Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All ConMed Corporation recalls
8 shown- Lower riskMedical device
ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture
ConMed recalls 5.5mm GENESYS CrossFT Suture Anchors with possible incorrect patient implant cards, risking wrong device identification. Affected units have specific reference numbers.
ConMedJul 14, 2026 - Lower riskMedical device
ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per
ConMed recalls 12mm AirSeal Access Ports with potential overpressure alerts. Affected units have specific catalog numbers and production dates. Consumers should contact ConMed for details.
ConMedMay 14, 2026 - Use cautionMedical device
ConMed Corporation recalls Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
ConMed recalls Electrosurgical Suction Coagulators 10FR with potential suction port occlusion, risking procedure delays. Affected units have specific lot codes and catalog numbers.
ConMedNov 18, 2022 - Lower riskMedical device
ConMed Corporation recalls KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and Tip Guides product line,
ConMed recalls certain KIT_INFINITY_BASE Custom Procedural Kits for possible lateral misalignment of tip guides, which may delay surgery or require alternative procedures.
ConMedMar 26, 2021 - Lower riskMedical device
ConMed Corporation recalls Infinity ACL Tibial Tip Guide- indicated for use in open and arthroscopic procedures for knee ligament reconstruction.
ConMed recalls Infinity ACL Tibial Tip Guides for possible lateral misalignment during knee ligament surgery. Affected units have specific catalog numbers and lot codes. Contact ConMed for details.
ConMedNov 12, 2020 - Lower riskMedical device
Conmed Corporation recalls ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval
ConMed recalls specific surgical pouches due to potential sterility compromise from seal defects. Affected units manufactured between April 2018 and February 2019 with certain lot codes.
ConMedMar 21, 2019 - Lower riskMedical device
ConMed Corporation recalls MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control¿ Quik-Combo" Connector, REF/Catalog Number 2602M
ConMed recalls Mini Infant < 3kg Radiotranslucent Electrodes with adhesive on contact wires that may impede conductivity and cause device failure. Affected units include specific lot numbers.
ConMedFeb 23, 2018 - Lower riskMedical device
ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog
ConMed recalls STAT 2.5 I.V. gravity flow controllers and administration sets due to inconsistent fluid flow rates. Affected units include specific catalog numbers and production dates from April 2012 to February 2017.
ConMedJun 19, 2017
ConMed Corporation recall questions
How many recalls has ConMed Corporation had?
30 recalls from ConMed Corporation are on record with U.S. safety agencies, from 2017–2026.
What is the most recent ConMed Corporation recall?
ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture, dated Jul 14, 2026. Every ConMed Corporation recall is listed on this page, newest first.
Why are ConMed Corporation products recalled?
The most common reasons on record: Potential for overpressure alerts. (11).
What should I do if I have a recalled ConMed Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new ConMed Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.