Aesculap recalls

Aesculap has 42 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 11 Mar 2026. 20 are still ongoing. 5 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls42since 2012

Last 12 months5reported

Class I00% of total

Ongoing20latest 11 Mar 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 5 0 0May 0 0 0Aug 0 2 4Nov 0 0 0Feb 1 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 41 98%Class III 1 2%

Why aesculap is recalled

Product types

By year

202612%
20251126%
2024819%
201625%
2015614%
2014614%
2013717%
201212%

Ongoing aesculap recalls

20 active

Reported	Class	Recall	Company	Reason	Where
11 Mar 2026Device	CLASS II	Minop Trocar 4 Wking Channel6 recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
5 Nov 2025Device	CLASS II	Sealing Unit For Trocars recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
5 Nov 2025Device	CLASS II	Sealing Cap For Trocars recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
5 Nov 2025Device	CLASS II	Reducing Converter recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
5 Nov 2025Device	CLASS II	Sealing Unit F/ Trocars W.reducer recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
8 Oct 2025Device	CLASS II	Elan 4 Fixed Duraguard Long recalled by Aesculap AG	Aesculap	Labeling Errors	MO

All aesculap recalls, newest first

42 total

Reported	Class	Recall	Company	Reason	Where
11 Mar 2026Device	CLASS II	Minop Trocar 4 Wking Channel6 recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
5 Nov 2025Device	CLASS II	Sealing Unit For Trocars recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
5 Nov 2025Device	CLASS II	Sealing Cap For Trocars recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
5 Nov 2025Device	CLASS II	Reducing Converter recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
5 Nov 2025Device	CLASS II	Sealing Unit F/ Trocars W.reducer recalled by Aesculap	Aesculap	Packaging Defects	Nationwide
8 Oct 2025Device	CLASS II	Elan 4 Fixed Duraguard Long recalled by Aesculap AG	Aesculap	Labeling Errors	MO
8 Oct 2025Device	CLASS II	Elan 4 Fixed Duraguard Standard recalled by Aesculap AG	Aesculap	Labeling Errors	MO
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BH198R recalled	Aesculap	Device Malfunction	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF FB458R recalled	Aesculap	Device Malfunction	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BH100R recalled	Aesculap	Device Malfunction	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R recalled	Aesculap	Device Malfunction	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BH951R recalled	Aesculap	Device Malfunction	Nationwide
19 Jun 2024Device	CLASS II	Aeos Robotic Digital Microscope, Product recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
13 Mar 2024Device	CLASS II	Disp.Hasson Trocar, Product recalled by Aesculap	Aesculap	Sterility	Nationwide
13 Mar 2024Device	CLASS II	Disp.trocar W recalled by Aesculap	Aesculap	Sterility	Nationwide
13 Mar 2024Device	CLASS II	Disp.Trocar W.Dilating Pin, Product recalled by Aesculap	Aesculap	Sterility	Nationwide
13 Mar 2024Device	CLASS II	Disp.Trocar W.Dilating Pin, Product recalled by Aesculap	Aesculap	Sterility	Nationwide
13 Mar 2024Device	CLASS II	Disp.Hasson Trocar, Product recalled by Aesculap	Aesculap	Sterility	Nationwide
7 Feb 2024Device	CLASS II	MB362R - Jacobson Durogrip TC Micro Needle Holder, straight recalled	Aesculap	Other	Nationwide
7 Feb 2024Device	CLASS II	MB215R - Mills Durogrip TC Micro Needle Holder, straight recalled	Aesculap	Other	Nationwide
9 Mar 2016Device	CLASS II	Columbus Revision Knee System, EnduRo Knee System recalled by Aesculap	Aesculap	Sterility	Nationwide
6 Jan 2016Device	CLASS II	Valve XS Atrium Retractor FC429R 52154756 The Valve XS recalled	Aesculap	Sterility	NY
30 Dec 2015Device	CLASS II	Flexible Bone Awl recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
30 Dec 2015Device	CLASS II	Tray Set containing multiple instruments recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
30 Dec 2015Device	CLASS II	Flexible Drill recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
30 Dec 2015Device	CLASS II	Flexible Screw Driver SJ706R recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
12 Aug 2015Device	CLASS II	S4C Occiput Torque Wrench F/Set Screw recalled by Aesculap	Aesculap	Device Malfunction	Nationwide
4 Feb 2015Device	CLASS II	Miethke Shunt System accessories recalled by Aesculap	Aesculap	Other	Nationwide
24 Dec 2014Device	CLASS III	Miethke Shunt System, miniNAV Valve recalled by Aesculap	Aesculap	Other	OK, WI
10 Dec 2014Device	CLASS II	The Dual Switch Valve is used recalled by Aesculap	Aesculap	Sterility	KS

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.