--- title: "Peter Lazic Gmbh Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Peter Lazic Gmbh recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/peter-lazic-gmbh/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Peter Lazic Gmbh recall records **5** reported ongoing 5 records in this archive. Latest source date Oct 6, 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 Oct 6, 2023 FDA device enforcement ### [D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.](https://isitonrecall.com/recall/fda-device-z-1277-2024-d-clip-standard-mini-applier-190mm-bayonet-jaw-rigid-double-action/) Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. Class II Reported ongoing Distribution: US Nationwide distribution in the state of ME. [Official source for D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1277-2024%22) Oct 6, 2023 FDA device enforcement ### [D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.](https://isitonrecall.com/recall/fda-device-z-1278-2024-d-clip-standard-mini-applier-210mm-bayonet-jaw-rigid-double-action/) Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. Class II Reported ongoing Distribution: US Nationwide distribution in the state of ME. [Official source for D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1278-2024%22) Oct 6, 2023 FDA device enforcement ### [D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.](https://isitonrecall.com/recall/fda-device-z-1279-2024-d-clip-standard-mini-applier-230mm-bayonet-jaw-rigid-double-action/) Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. Class II Reported ongoing Distribution: US Nationwide distribution in the state of ME. [Official source for D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1279-2024%22) Jul 14, 2023 FDA device enforcement ### [L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile](https://isitonrecall.com/recall/fda-device-z-1287-2024-l-aneurysm-clip-titanium-paddle-clip-permanent-11-mm-straight-sterile/) Wrong product coloring. The paddle clips should be blank, but they are colored blue. Class II Reported ongoing Distribution: US Nationwide distribution in the state of ME. [Official source for L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1287-2024%22) Jul 14, 2023 FDA device enforcement ### [L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile](https://isitonrecall.com/recall/fda-device-z-1288-2024-l-aneurysm-clip-titanium-paddle-clip-permanent-11-mm-straight-non-sterile/) Wrong product coloring. The paddle clips should be blank, but they are colored blue. Class II Reported ongoing Distribution: US Nationwide distribution in the state of ME. [Official source for L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1288-2024%22) ## Reasons in these listed records - Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. - Wrong product coloring. The paddle clips should be blank, but they are colored blue. These examples come from this result page and are not a ranking of every recall reason. ## Checking Peter Lazic Gmbh ### Is there a recall on peter lazic gmbh right now? This archive contains 5 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 Peter Lazic Gmbh](https://isitonrecall.com/check/?q=Peter%20Lazic%20Gmbh) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)