Aesculap Implant Systems recalls

Aesculap Implant Systems has 61 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 13 Sep 2023. 5 are still ongoing. The most frequent reason is device malfunction.

Total recalls61since 2012

Last 12 months0reported

Class I00% of total

Ongoing5latest 13 Sep 2023

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 59 97%Class III 2 3%

Why aesculap implant systems is recalled

Product types

By year

202347%
20221931%
20211016%
202047%
201923%
20181118%
2017610%
201612%
201247%

Ongoing aesculap implant systems recalls

5 active

Reported	Class	Recall	Company	Reason	Where
13 Sep 2023Device	CLASS II	For intraventricular recalled by Aesculap Implant Systems	Aesculap Implant Systems	Device Malfunction	Nationwide
26 Jul 2023Device	CLASS II	Aesculap Surgical Needle, straight, 3 1/2", width recalled	Aesculap Implant Systems	Sterility	Nationwide
17 May 2023Device	CLASS II	Aesculap Caiman Articulating D5 recalled by Aesculap Implant Systems	Aesculap Implant Systems	Other	Nationwide
3 May 2023Device	CLASS II	Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only recalled	Aesculap Implant Systems	Labeling Errors	Nationwide
7 Sep 2022Device	CLASS II	Aesculap Ennovate Set Screw Sterile-implants are used recalled	Aesculap Implant Systems	Sterility	GA, TX

All aesculap implant systems recalls, newest first

61 total

Reported	Class	Recall	Company	Reason	Where
13 Sep 2023Device	CLASS II	For intraventricular recalled by Aesculap Implant Systems	Aesculap Implant Systems	Device Malfunction	Nationwide
26 Jul 2023Device	CLASS II	Aesculap Surgical Needle, straight, 3 1/2", width recalled	Aesculap Implant Systems	Sterility	Nationwide
17 May 2023Device	CLASS II	Aesculap Caiman Articulating D5 recalled by Aesculap Implant Systems	Aesculap Implant Systems	Other	Nationwide
3 May 2023Device	CLASS II	Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only recalled	Aesculap Implant Systems	Labeling Errors	Nationwide
7 Sep 2022Device	CLASS II	Aesculap Ennovate Set Screw Sterile-implants are used recalled	Aesculap Implant Systems	Sterility	GA, TX
17 Aug 2022Device	CLASS II	Aeos¿ Robotic Digital Microscope recalled by Aesculap Implant Systems	Aesculap Implant Systems	Device Malfunction	4 states
10 Aug 2022Device	CLASS II	Prestige Atraumatic Grasper W/port Dual Action, Rotating Diam recalled	Aesculap Implant Systems	Other	Nationwide
10 Aug 2022Device	CLASS II	Prestige Retraction Grasper, W/port Dual Action, Rotating Diam recalled	Aesculap Implant Systems	Other	Nationwide
27 Jul 2022Device	CLASS II	Aesculap Sterile disposable fleece drape, Product recalled	Aesculap Implant Systems	Sterility	14 states
27 Jul 2022Device	CLASS II	Aesculap S4 Cervical Cross Connector, L26mm recalled	Aesculap Implant Systems	Lead & Heavy Metals	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.