ConMed Corporation: 66 recalls on record

Recalls filed with 1 agency: FDA (66).

First recall on record: December 19, 2012. Most recent: September 2, 2026.

Risk classification: Class I: 9 · Class II: 57

Most recent recalls

DateAgencyProduct
September 2, 2026FDACONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5…Z-3018-2026
June 24, 2026FDAConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm…Z-2472-2026
June 24, 2026FDAConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Numbe…Z-2466-2026
June 24, 2026FDAConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120m…Z-2467-2026
June 24, 2026FDAConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Numb…Z-2465-2026
June 24, 2026FDAConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120…Z-2473-2026
June 24, 2026FDAConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120m…Z-2470-2026
June 24, 2026FDAConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalo…Z-2464-2026
June 24, 2026FDAConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100m…Z-2471-2026
June 24, 2026FDAConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100m…Z-2468-2026
June 24, 2026FDAConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm…Z-2469-2026
June 24, 2026FDAConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm…Z-2474-2026
May 5, 2021FDAKIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and…Z-1499-2021
May 15, 2019FDAConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 …Z-1305-2019
May 15, 2019FDAConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 …Z-1304-2019
March 7, 2018FDASTAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets a…Z-0804-2018
December 20, 2017FDANonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic…Z-0253-2018
April 19, 2017FDAHYFRECATOR 2000 HANDPIECE SHEATH, REF/Part Number 7-796-19, Rx ONLY, STERILE, Single Pati…Z-1760-2017
April 19, 2017FDASterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in …Z-1756-2017
April 19, 2017FDASterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in …Z-1758-2017
April 19, 2017FDASterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in …Z-1759-2017
October 26, 2016FDACORE¿ Trumpet Handpiece only, Catalog Number CD8450 The CORE Trumpet (CD81XX, CD83XX, an…Z-0135-2017
October 26, 2016FDACORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution Bags,…Z-0129-2017
October 26, 2016FDACORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags, Catalog Number…Z-0132-2017
October 26, 2016FDACORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution or D…Z-0130-2017

Questions about this company

How many recalls does ConMed Corporation have?
Recalert has 66 U.S. recalls on record for ConMed Corporation, published between December 19, 2012 and September 2, 2026.
What was the most recent ConMed Corporation recall?
FDA recall Z-3018-2026, published September 2, 2026: CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures Sterile
Which agencies have handled ConMed Corporation recalls?
ConMed Corporation appears as the recalling firm in recalls from: FDA (66).

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