Aesculap recalls

Aesculap has 40 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 11 Mar 2026. 18 are still ongoing. 5 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls40since 2012

Last 12 months5reported

Class I00% of total

Ongoing18latest 11 Mar 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 5 0Apr 0 0 0Jul 0 0 0Oct 4 0 0Jan '26 0 1 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 39 98%Class III 1 3%

Why aesculap is recalled

Product types

By year

202613%
2025923%
2024820%
201625%
2015615%
2014615%
2013718%
201213%

Ongoing aesculap recalls

18 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 To 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
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BH198R recalled	Aesculap	Sterility	Nationwide

All aesculap recalls, newest first

40 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 To 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
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BH198R recalled	Aesculap	Sterility	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF FB458R recalled	Aesculap	Sterility	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BH100R recalled	Aesculap	Sterility	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R recalled	Aesculap	Sterility	Nationwide
19 Mar 2025Device	CLASS II	Numerous models of nonsterile hemostatic forceps: (1) REF BH951R recalled	Aesculap	Sterility	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.