--- title: "Aesculap Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Aesculap Inc 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-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Aesculap Inc recall records **18** reported ongoing 18 records in this archive. Latest source date Jan 15, 2026. 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 Jan 15, 2026 FDA device enforcement ### [Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHA...](https://isitonrecall.com/recall/fda-device-z-1485-2026-brand-name-aesculap-product-name-minop-trocar-150mm-4-wking-channel6-0mm-model-catalog-number-ff399r/) There is the potential for the length of the trocar shaft to be too long. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, AR, CA, CO, FL, GA, HI, IA, ID, IL, KS, LA, MA, MD, MI, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TX, UT, WA. [Official source for Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1485-2026%22) Sep 24, 2025 FDA device enforcement ### [Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Version: N/A Product Description: SEALING UNIT F/10/12MM TROCAR...](https://isitonrecall.com/recall/fda-device-z-0309-2026-brand-name-aesculap-product-name-sealing-unit-f-10-12mm-trocars-w-reducer-model-catalog-number-ek083/) It was determined there is the potential of silicone fragments detaching from the yellow sealing component. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD, NE, NM, NY, OR, PA, WA, WI and the country of Canada. [Official source for Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number:...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0309-2026%22) Sep 24, 2025 FDA device enforcement ### [Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Model/Catalog Number: EK085P Software Version: N/A Product Description: SEALING CAP FOR 10/12MM TROCARS Compon...](https://isitonrecall.com/recall/fda-device-z-0310-2026-brand-name-aesculap-product-name-sealing-cap-for-10-12mm-trocars-model-catalog-number-ek085p-softwar/) It was determined there is the potential of silicone fragments detaching from the yellow sealing component. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD, NE, NM, NY, OR, PA, WA, WI and the country of Canada. [Official source for Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Model/Catalog Number: EK085P S...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0310-2026%22) Sep 24, 2025 FDA device enforcement ### [Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Model/Catalog Number: EK086P Software Version: N/A Product Description: SEALING UNIT FOR 10/12MM TROCARS Comp...](https://isitonrecall.com/recall/fda-device-z-0311-2026-brand-name-aesculap-product-name-sealing-unit-for-10-12mm-trocars-model-catalog-number-ek086p-softwa/) It was determined there is the potential of silicone fragments detaching from the yellow sealing component. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD, NE, NM, NY, OR, PA, WA, WI and the country of Canada. [Official source for Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Model/Catalog Number: EK086P ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0311-2026%22) Sep 24, 2025 FDA device enforcement ### [Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A Product Description: REDUCING CONVERTER 10/12MM TO 5MM Co...](https://isitonrecall.com/recall/fda-device-z-0312-2026-brand-name-aesculap-product-name-reducing-converter-10-12mm-to-5mm-model-catalog-number-ek087p-softw/) It was determined there is the potential of silicone fragments detaching from the yellow sealing component. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD, NE, NM, NY, OR, PA, WA, WI and the country of Canada. [Official source for Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0312-2026%22) Jan 31, 2025 FDA device enforcement ### [Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hysterectomy Forceps ANG 205MM; (3) REF BJ511R,...](https://isitonrecall.com/recall/fda-device-z-1308-2025-numerous-models-of-nonsterile-hemostatic-forceps-1-ref-bj500r-phaneuf-hysterectomy-forceps-str-210mm/) The forceps have been used in ways not covered by the design resulting in breakage of the clamps. Class II Reported ongoing Distribution: Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar. [Official source for Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps ST...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1308-2025%22) Jan 31, 2025 FDA device enforcement ### [Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery Forceps 85MM; (2) REF BH104R, Hartmann Mosquito FCSDEL STR 100MM; (3) REF BH105R, Hartmann Mosqui...](https://isitonrecall.com/recall/fda-device-z-1309-2025-numerous-models-of-nonsterile-hemostatic-forceps-1-ref-bh100r-carrel-artery-forceps-85mm-2-ref-bh104/) The forceps have been used in ways not covered by the design resulting in breakage of the clamps. Class II Reported ongoing Distribution: Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar. [Official source for Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery Forceps 85MM; (2)...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1309-2025%22) Jan 31, 2025 FDA device enforcement ### [Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery Forceps CVD.190MM; (2) REF BH304R, Pean Artery Forceps Straight 140MM; (3) REF BH813R, Artery Fo...](https://isitonrecall.com/recall/fda-device-z-1310-2025-numerous-models-of-nonsterile-hemostatic-forceps-1-ref-bh198r-fuchsig-artery-forceps-cvd-190mm-2-ref/) The forceps have been used in ways not covered by the design resulting in breakage of the clamps. Class II Reported ongoing Distribution: Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar. [Official source for Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery Forceps CVD.190M...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1310-2025%22) Jan 31, 2025 FDA device enforcement ### [Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP CVD 215MM; (2) REF FB459R, Glover ATR.CLAMP CVD 245MM; (3) REF FB461R, Glover ATR.CLAMP 195MM;...](https://isitonrecall.com/recall/fda-device-z-1311-2025-numerous-models-of-nonsterile-hemostatic-forceps-1-ref-fb458r-glover-atr-clamp-cvd-215mm-2-ref-fb459/) The forceps have been used in ways not covered by the design resulting in breakage of the clamps. Class II Reported ongoing Distribution: Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar. [Official source for Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP CVD 215MM; (2)...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1311-2025%22) Jan 31, 2025 FDA device enforcement ### [Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps X-HVY-CVD190MM; (3) REF BH957R, Schnid...](https://isitonrecall.com/recall/fda-device-z-1312-2025-numerous-models-of-nonsterile-hemostatic-forceps-1-ref-bh951r-negus-tonsil-forceps-hvy-cvd-190mm-2-r/) The forceps have been used in ways not covered by the design resulting in breakage of the clamps. Class II Reported ongoing Distribution: Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar. [Official source for Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 19...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1312-2025%22) May 13, 2024 FDA device enforcement ### [Aeos Robotic Digital Microscope, Product Code: PV010](https://isitonrecall.com/recall/fda-device-z-2139-2024-aeos-robotic-digital-microscope-product-code-pv010/) Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AR, FL, IL, IN, KY, MI, NC, NE, OK, SD, TX. [Official source for Aeos Robotic Digital Microscope, Product Code: PV010](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2139-2024%22) Jan 9, 2024 FDA device enforcement ### [DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic procedures.](https://isitonrecall.com/recall/fda-device-z-1243-2024-disp-trocar-w-dilating-pin-10-110mm-product-code-ek224su-for-use-in-laparoscopic-procedures/) The sterile blister packaging may be damaged, and sterility may be compromised. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada. [Official source for DISP.TROCAR W. DILATING PIN 10/110MM, Product Code EK224SU. For use in laparoscopic procedures.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1243-2024%22) Jan 9, 2024 FDA device enforcement ### [DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.](https://isitonrecall.com/recall/fda-device-z-1244-2024-disp-hasson-trocar-10-110mm-product-code-ek230su-for-use-in-laparoscopic-procedures/) The sterile blister packaging may be damaged, and sterility may be compromised. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada. [Official source for DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1244-2024%22) Jan 9, 2024 FDA device enforcement ### [DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.](https://isitonrecall.com/recall/fda-device-z-1245-2024-disp-trocar-w-dilating-pin-12-110mm-product-code-ek234su-for-use-in-laparoscopic-procedures/) The sterile blister packaging may be damaged, and sterility may be compromised. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada. [Official source for DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1245-2024%22) Jan 9, 2024 FDA device enforcement ### [DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures.](https://isitonrecall.com/recall/fda-device-z-1246-2024-disp-trocar-w-dilating-pin-12-110mm-product-code-ek236su-for-use-in-laparoscopic-procedures/) The sterile blister packaging may be damaged, and sterility may be compromised. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada. [Official source for DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1246-2024%22) Jan 9, 2024 FDA device enforcement ### [DISP.HASSON TROCAR 12/110MM, Product Code EK240SU. For use in laparoscopic procedures.](https://isitonrecall.com/recall/fda-device-z-1247-2024-disp-hasson-trocar-12-110mm-product-code-ek240su-for-use-in-laparoscopic-procedures/) The sterile blister packaging may be damaged, and sterility may be compromised. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada. [Official source for DISP.HASSON TROCAR 12/110MM, Product Code EK240SU. For use in laparoscopic procedures.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1247-2024%22) Dec 29, 2023 FDA device enforcement ### [MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";](https://isitonrecall.com/recall/fda-device-z-0866-2024-mb362r-jacobson-durogrip-tc-micro-needle-holder-straight-8-3-4-220-mm-tc-jacobson-ndl-hld-str-jaw-22/) Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, CO, FL, ID, KY, MD, MO, MT, NV, NY, OR, PA, RI, TN, TX, VA. [Official source for MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL H...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0866-2024%22) Dec 29, 2023 FDA device enforcement ### [MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND HNDLSTR203MM"](https://isitonrecall.com/recall/fda-device-z-0867-2024-mb215r-mills-durogrip-tc-micro-needle-holder-straight-8-203-mm-tc-mills-ndle-holdrrnd-hndlstr203mm/) Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, CO, FL, ID, KY, MD, MO, MT, NV, NY, OR, PA, RI, TN, TX, VA. [Official source for MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND H...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0867-2024%22) ## Reasons in these listed records - There is the potential for the length of the trocar shaft to be too long. - It was determined there is the potential of silicone fragments detaching from the yellow sealing component. - The forceps have been used in ways not covered by the design resulting in breakage of the clamps. - Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism. These examples come from this result page and are not a ranking of every recall reason. ## Checking Aesculap Inc ### Is there a recall on aesculap inc right now? This archive contains 18 records, including 18 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 Inc](https://isitonrecall.com/check/?q=Aesculap%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)