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

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 11 0Jul 0 1

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	Sterility	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	Sterility	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

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.