ConMed recalls

ConMed has 92 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 2 Sep 2026. 12 are still ongoing. 12 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls92since 2012

Last 12 months12reported

Class I910% of total

Ongoing12latest 2 Sep 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 11 0 0Aug 1 0

Severity split

Class I 9 10%Class II 83 90%Class III 0 0%

Why conmed is recalled

Product types

By year

20261213%
202211%
202122%
202022%
201967%
201878%
201767%
20161415%
201522%
20141112%

Ongoing conmed recalls

12 active

Reported	Class	Recall	Company	Reason	Where
2 Sep 2026Device	CLASS II	Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled	ConMed	Other	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Palm Grip Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Obturator with Blunt Tip Length recalled	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Palm Grip Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide

All conmed recalls, newest first

92 total

Reported	Class	Recall	Company	Reason	Where
2 Sep 2026Device	CLASS II	Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled	ConMed	Other	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Palm Grip Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Obturator with Blunt Tip Length recalled	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Palm Grip Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Smooth Access Port and Obturator with Blunt Tip Length recalled	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Low Profile Obturator recalled by ConMed	ConMed	Packaging Defects	Nationwide
24 Jun 2026Device	CLASS II	AirSeal Access Port and Obturator with Blunt Tip Length recalled	ConMed	Packaging Defects	Nationwide
21 Dec 2022Device	CLASS II	Foot Controlled Electrosurgical Suction Coagulator recalled by ConMed	ConMed	Other	Nationwide
5 May 2021Device	CLASS II	INFINITY_TRAY Custom Procedural Kit - Canada recalled by ConMed	ConMed	Other	NY
5 May 2021Device	CLASS II	KIT_INFINITY_BASE Custom Procedural Kit - Italy recalled by ConMed	ConMed	Other	NY
30 Dec 2020Device	CLASS II	Infinity ACL Tibial Elbow Guide-indicated for use recalled by ConMed	ConMed	Other	Nationwide
30 Dec 2020Device	CLASS II	Infinity ACL Tibial Tip Guide- indicated for use in open recalled	ConMed	Other	Nationwide
15 May 2019Device	CLASS II	Anchor Tissue Retrieval System" (5/BX) recalled by Conmed	Conmed	Sterility	Nationwide
15 May 2019Device	CLASS II	Anchor Tissue Retrieval System (5/BX) recalled by Conmed	Conmed	Sterility	Nationwide
15 May 2019Device	CLASS II	Anchor Tissue Retrieval System (3/BX) recalled by Conmed	Conmed	Sterility	Nationwide
15 May 2019Device	CLASS II	Anchor Tissue Retrieval System, VATS (3/BX) recalled by Conmed	Conmed	Sterility	Nationwide
15 May 2019Device	CLASS II	Anchor Tissue Retrieval System (3/BX) recalled by Conmed	Conmed	Sterility	Nationwide
15 May 2019Device	CLASS II	Anchor Tissue Retrieval System, (5/BX) recalled by Conmed	Conmed	Sterility	Nationwide
4 Apr 2018Device	CLASS II	Mini Infant <, Radiotranslucent Electrode recalled by ConMed	ConMed	Device Malfunction	Nationwide
4 Apr 2018Device	CLASS II	Mini Infant <, Radiotranslucent Electrode, Zoll¿ Connector recalled	ConMed	Device Malfunction	Nationwide
4 Apr 2018Device	CLASS II	Mini Infant <, Radiotranslucent Electrode recalled by ConMed	ConMed	Device Malfunction	Nationwide
4 Apr 2018Device	CLASS II	Mini Infant <, Radiotranslucent Electrode recalled by ConMed	ConMed	Device Malfunction	Nationwide
4 Apr 2018Device	CLASS II	Mini Infant <, Radiotranslucent Electrode recalled by ConMed	ConMed	Device Malfunction	Nationwide
7 Mar 2018Device	CLASS II	STAT 2¿ I.V recalled by ConMed	ConMed	Labeling Errors	Nationwide
7 Mar 2018Device	CLASS II	STAT 2¿ I.V recalled by ConMed	ConMed	Labeling Errors	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.