--- title: "Zimmer Surgical Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Zimmer Surgical 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/zimmer-surgical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Zimmer Surgical Inc recall records **8** reported ongoing 8 records in this archive. Latest source date Jun 9, 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 Jun 9, 2026 FDA device enforcement ### [Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors Model/Catalog Number: 60-1812-101-00 Software Version: N/A Pro...](https://isitonrecall.com/recall/fda-device-z-2673-2026-brand-name-sterile-tourniquet-hoses-product-name-a-t-s-4000-ts-tourniquet-systems-dual-hose-with-cpc/) Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada and EMEA. [Official source for Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose wi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2673-2026%22) Jun 9, 2026 FDA device enforcement ### [Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose with CPC Connectors Model/Catalog Number: 60-4009-101-00 Software Version: N/A P...](https://isitonrecall.com/recall/fda-device-z-2674-2026-brand-name-sterile-tourniquet-hoses-product-name-a-t-s-4000-ts-tourniquet-systems-single-hose-with-c/) Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada and EMEA. [Official source for Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2674-2026%22) Dec 24, 2025 FDA device enforcement ### [Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software version v2.04 or prior are wit...](https://isitonrecall.com/recall/fda-device-z-1201-2026-brand-name-zimmer-tourniquet-systems-product-name-a-t-s-5000ts-tourniquet-systems-model-catalog-numb/) Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located. Class II Reported ongoing Distribution: International distribution to the countries of Canada and EMEA only. [Official source for Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catal...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1201-2026%22) Dec 24, 2025 FDA device enforcement ### [Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are wit...](https://isitonrecall.com/recall/fda-device-z-1202-2026-brand-name-zimmer-tourniquet-systems-product-name-a-t-s-3200ts-tourniquet-systems-model-catalog-numb/) Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located. Class II Reported ongoing Distribution: International distribution to the countries of Canada and EMEA only. [Official source for Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catal...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1202-2026%22) Nov 24, 2025 FDA device enforcement ### [Zimmer Air Dermatome, Model/Catalog Number: 00880100100](https://isitonrecall.com/recall/fda-device-z-0924-2026-zimmer-air-dermatome-model-catalog-number-00880100100/) The devices may have a misaligned thickness control bar. Class II Reported ongoing Distribution: Distribution regions: USA, Hong Kong, Thailand, Japan, Korea, Australia, Taiwan, India, Malaysia, Singapore, China, Canada, EMEA, Mexico, Trinidad & Tobago, Panama, Guatemala Re... [Official source for Zimmer Air Dermatome, Model/Catalog Number: 00880100100](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0924-2026%22) Nov 24, 2025 FDA device enforcement ### [Zimmer Dermatome AN, Model/Catalog Number: 88710100](https://isitonrecall.com/recall/fda-device-z-0925-2026-zimmer-dermatome-an-model-catalog-number-88710100/) The devices may have a misaligned thickness control bar. Class II Reported ongoing Distribution: Distribution regions: USA, Hong Kong, Thailand, Japan, Korea, Australia, Taiwan, India, Malaysia, Singapore, China, Canada, EMEA, Mexico, Trinidad & Tobago, Panama, Guatemala Re... [Official source for Zimmer Dermatome AN, Model/Catalog Number: 88710100](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0925-2026%22) Jan 2, 2024 FDA device enforcement ### [3:1 Dermacarrier, Model Number 00219501300, skin graft carrier](https://isitonrecall.com/recall/fda-device-z-1078-2024-3-1-dermacarrier-model-number-00219501300-skin-graft-carrier/) Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of CA, DE, FL, GA, IA, IL, IN, KS, LA, MI, MO, MT, NC, NV, NY, OH, OK, PA, RI, TN, TX, UT, VA, WA, WI, WV and the ... [Official source for 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1078-2024%22) Sep 5, 2023 FDA device enforcement ### [Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting instrument that is intended to provide variable graft th...](https://isitonrecall.com/recall/fda-device-z-0069-2024-zimmer-dermatome-blades-10-pack-boxes-of-blades-intended-for-use-with-the-dermatome-handpiece-which/) Skin grafts thin and non-uniform when using the affected blades. The issue would be identified at the time of use and may result in the need for additional harvests to adequately cover the area Class II Reported ongoing Distribution: US Nationwide Foreign: AUSTRALIA BRAZIL CHINA HONG KONG INDIA JAPAN MALAYSIA MEXICO NETHERLANDS ON SEOUL SINGAPORE TAIWAN THAILAND [Official source for Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece w...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0069-2024%22) ## Reasons in these listed records - Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device. - Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located. - The devices may have a misaligned thickness control bar. - Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary. These examples come from this result page and are not a ranking of every recall reason. ## Checking Zimmer Surgical Inc ### Is there a recall on zimmer surgical inc right now? This archive contains 8 records, including 8 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 Zimmer Surgical Inc](https://isitonrecall.com/check/?q=Zimmer%20Surgical%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)