Epimed International recalls

Epimed International has 11 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 25 Aug 2021. The most frequent reason is sterility.

Total recalls11since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 25 Aug 2021

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 0 0Jul 0 0

Severity split

Class I 0 0%Class II 11 100%Class III 0 0%

Why epimed international is recalled

Product types

By year

2021327%
2020218%
2019218%
2017327%
201619%

All epimed international recalls, newest first

11 total

Reported	Class	Recall	Company	Reason	Where
25 Aug 2021Device	CLASS II	Neo-kath Epidural Catheter Set recalled by Epimed International	Epimed International	Sterility	Nationwide
25 Aug 2021Device	CLASS II	Neo-kath(TM) Caudal Set recalled by Epimed International	Epimed International	Sterility	Nationwide
24 Mar 2021Device	CLASS II	Feth-R-Kath Catheter recalled by Epimed International	Epimed International	Device Malfunction	Nationwide
13 May 2020Device	CLASS II	R-F Injector Cannula recalled by Epimed International	Epimed International	Sterility	Nationwide
13 May 2020Device	CLASS II	R-F Injector Cannula recalled by Epimed International	Epimed International	Sterility	Nationwide
31 Jul 2019Device	CLASS II	Versa - Kath Mini Kit, with plastic L.O.R Syringe, Sterile ED recalled	Epimed International	Labeling Errors	8 states
31 Jul 2019Device	CLASS II	Versa - Kath Mini Kit, with plastic L.O.R Syringe, Sterile ED recalled	Epimed International	Labeling Errors	8 states
15 Nov 2017Device	CLASS II	Coude Blunt Nerve Block Needle recalled by Epimed International	Epimed International	Sterility	13 states
15 Nov 2017Device	CLASS II	Tuohy Epidural Needle TW, Calibrated, Plastic Hub recalled	Epimed International	Foreign Material	13 states
15 Nov 2017Device	CLASS II	RX-2 Coude Epidural NeedleTW, Calibrated, Plastic Hub recalled	Epimed International	Foreign Material	13 states

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.