Covidien LP

Covidien LP holds 4 FDA 510(k) medical device clearances, first cleared 2009, most recent 2026, with 131 FDA device recalls on record.

Top product codes for Covidien LP

FDA recalls by Covidien LP

10 most recent of 131

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by Covidien LP

Data sourced from openFDA. This site is unofficial and independent of the FDA.