--- title: "Aesculap Implant Systems LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Aesculap Implant Systems LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/aesculap-implant-systems-llc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Aesculap Implant Systems LLC recall records **5** reported ongoing 7 records in this archive. Latest source date Jul 20, 2023. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jul 20, 2023 FDA device enforcement ### [For intraventricular indications mainly used for operations within the brain ventricles. Product Code: FF399R](https://isitonrecall.com/recall/fda-device-z-2518-2023-for-intraventricular-indications-mainly-used-for-operations-within-the-brain-ventricles-product-code/) Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30¿ neuroendoscope, a portion of the visual field is obscured. Class II Reported ongoing Distribution: US Nationwide distribution in the states of FL, ID, IL, MD, NC, NY, OR, RI, TX. [Official source for For intraventricular indications mainly used for operations within the brain ventricles. Product ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2518-2023%22) May 18, 2023 FDA device enforcement ### [Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable Article Number: MD610](https://isitonrecall.com/recall/fda-device-z-2146-2023-aesculap-surgical-needle-straight-3-1-2-90-mm-13ga-width-2-400-mm-non-sterile-reusable-article-numbe/) Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610. Class II Reported ongoing Distribution: US Nationwide distribution in the states of DC, MO, PA, TX. [Official source for Aesculap Surgical Needle, straight, 3 1/2", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2146-2023%22) Mar 21, 2023 FDA device enforcement ### [Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopi...](https://isitonrecall.com/recall/fda-device-z-1569-2023-aesculap-caiman-articulating-d5-360mm-an-electrosurgical-cutting-and-coagulation-device-for-cutting/) Potential for the spring to become loose and fall out of the device, if the spring falls out during a surgical procedure, it may enter the patient's body. Class II Reported ongoing Distribution: US Nationwide distribution in the state of OH. [Official source for Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cut...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1569-2023%22) Feb 23, 2023 FDA device enforcement ### [Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and ME764 Casper Cervical Retractor (CCR) Basket Full System - Lid Only. A lid to a container intended to provide a suita...](https://isitonrecall.com/recall/fda-device-z-1430-2023-caspar-cervical-retractor-ccr-basket-me754-lid-only-and-me764-casper-cervical-retractor-ccr-basket-f/) Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct GTIN # is 04046955299607. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, OH, NE, NH, FL, PA, TX. [Official source for Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and ME764 Casper Cervical Retractor (CCR)...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1430-2023%22) Jul 15, 2022 FDA device enforcement ### [Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar, thoracic and sacral spine. Article Number: 52758014](https://isitonrecall.com/recall/fda-device-z-1638-2022-aesculap-ennovate-set-screw-sterile-implants-are-used-for-dorsal-monosegmental-and-multisegmental-st/) Potential for the incorrect screw to be included in the package. Class II Reported ongoing Distribution: GA, TX [Official source for Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1638-2022%22) Jul 14, 2022 FDA device enforcement ### [Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010](https://isitonrecall.com/recall/fda-device-z-1516-2022-aeos-robotic-digital-microscope-with-software-versions-2-7-or-earlier-article-number-pv010/) Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available: Class II Reported terminated Distribution: US Distribution to states of: AR, IN, NE and NC [Official source for Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1516-2022%22) Oct 25, 2021 FDA device enforcement ### [MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441](https://isitonrecall.com/recall/fda-device-z-1410-2022-modulift-vbr-sz-m-4mm-set-screw-driver-mf790r-part-of-modulift-vbr-medium-instrument-set-st-0441/) Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant. Class II Reported terminated Distribution: US: CA, FL, GA, IL, OH & MI [Official source for MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1410-2022%22) ## Reasons in these listed records - Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30¿ neuroendoscope, a portion of the visual field is obscured. - Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610. - Potential for the spring to become loose and fall out of the device, if the spring falls out during a surgical procedure, it may enter the patient's body. - Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct GTIN # is 04046955299607. These examples come from this result page and are not a ranking of every recall reason. ## Checking Aesculap Implant Systems LLC ### Is there a recall on aesculap implant systems llc right now? This archive contains 7 records, including 5 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Aesculap Implant Systems LLC](https://isitonrecall.com/check/?q=Aesculap%20Implant%20Systems%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)