--- title: "Synergetics Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Synergetics 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/synergetics-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Synergetics Inc recall records **4** reported ongoing 4 records in this archive. Latest source date Jun 12, 2024. 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 12, 2024 FDA device enforcement ### [BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)](https://isitonrecall.com/recall/fda-device-z-2251-2024-bausch-lomb-i-pack-injection-kit-ref-18060-for-the-administration-of-intravitreal-injection-eye/) Sterilization certificates could not be validated by the supplier Class I Reported ongoing Distribution: US Nationwide [Official source for BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2251-2024%22) Jun 12, 2024 FDA device enforcement ### [BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)](https://isitonrecall.com/recall/fda-device-z-2252-2024-bausch-lomb-i-pack-injection-kit-with-drape-ref-18061-for-the-administration-of-intravitreal-injecti/) Sterilization certificates could not be validated by the supplier Class I Reported ongoing Distribution: US Nationwide [Official source for BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal i...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2252-2024%22) Jun 12, 2024 FDA device enforcement ### [BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)](https://isitonrecall.com/recall/fda-device-z-2253-2024-bausch-lomb-i-pack-injection-kit-custom-ref-18069-for-the-administration-of-intravitreal-injection-e/) Sterilization certificates could not be validated by the supplier Class I Reported ongoing Distribution: US Nationwide [Official source for BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injec...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2253-2024%22) Jun 12, 2024 FDA device enforcement ### [BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)](https://isitonrecall.com/recall/fda-device-z-2254-2024-bausch-lomb-i-pack-injection-kit-with-wire-speculum-ref-18069w-for-the-administration-of-intravitrea/) Sterilization certificates could not be validated by the supplier Class I Reported ongoing Distribution: US Nationwide [Official source for BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intra...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2254-2024%22) ## Reasons in these listed records - Sterilization certificates could not be validated by the supplier These examples come from this result page and are not a ranking of every recall reason. ## Checking Synergetics Inc ### Is there a recall on synergetics inc right now? This archive contains 4 records, including 4 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 Synergetics Inc](https://isitonrecall.com/check/?q=Synergetics%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)