--- title: "Vitae Enim Vitae Scientific, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Vitae Enim Vitae Scientific, 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/vitae-enim-vitae-scientific-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Vitae Enim Vitae Scientific, Inc. recall records **0** reported ongoing 4 records in this archive. Latest source date Mar 14, 2022. 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 Mar 14, 2022 FDA drug enforcement ### [TETRACAINE 1% Tetracaine HCI Injection, USP, 20mg/2mL (10mg/mL), 10 x 2ml Single Use Vials per box, Rx only, Manufactured for Cameron Pharmaceuticals, LLC., NDC 42494-437-10.](https://isitonrecall.com/recall/fda-drug-d-0741-2022-tetracaine-1-tetracaine-hci-injection-usp-20mg-2ml-10mg-ml-10-x-2ml-single-use-vials-per-box-rx-only/) Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile. Class II Reported terminated Distribution: Nationwide in the U.S.A [Official source for TETRACAINE 1% Tetracaine HCI Injection, USP, 20mg/2mL (10mg/mL), 10 x 2ml Single Use Vials per bo...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0741-2022%22) Mar 14, 2022 FDA drug enforcement ### [PAPAVERINE HYDROCHLORIDE Injection, USP, 60 mg/2mL (30 mg/mL), packaged as a) 25 x 2mL Single Use Vials per box (NDC 72516-024-25) and b) 10 x 2mL Single Use Vials per box (NDC ...](https://isitonrecall.com/recall/fda-drug-d-0742-2022-papaverine-hydrochloride-injection-usp-60-mg-2ml-30-mg-ml-packaged-as-a-25-x-2ml-single-use-vials-pe/) Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile. Class II Reported terminated Distribution: Nationwide in the U.S.A [Official source for PAPAVERINE HYDROCHLORIDE Injection, USP, 60 mg/2mL (30 mg/mL), packaged as a) 25 x 2mL Single Use...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0742-2022%22) Mar 14, 2022 FDA drug enforcement ### [PHENOBARBITAL Sodium Injection, USP, 65mg/mL, packaged as a) 25 x 1 mL Vials per box (NDC 42494-415-25) and b) 3 x 1 mL Vials per box (NDC 42494-415-03), Rx only, Manufactured f...](https://isitonrecall.com/recall/fda-drug-d-0743-2022-phenobarbital-sodium-injection-usp-65mg-ml-packaged-as-a-25-x-1-ml-vials-per-box-ndc-42494-415-25-an/) Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile. Class II Reported terminated Distribution: Nationwide in the U.S.A [Official source for PHENOBARBITAL Sodium Injection, USP, 65mg/mL, packaged as a) 25 x 1 mL Vials per box (NDC 42494-4...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0743-2022%22) Mar 14, 2022 FDA drug enforcement ### [PHENOBARBITAL Sodium Injection, USP, 130 mg/mL, packaged as a) 25 x 1 mL Vials per box (NDC 42494-416-25) and b) 3 x 1mL Vials per box (NDC 42494-416-03), Rx only, Manufactured ...](https://isitonrecall.com/recall/fda-drug-d-0744-2022-phenobarbital-sodium-injection-usp-130-mg-ml-packaged-as-a-25-x-1-ml-vials-per-box-ndc-42494-416-25/) Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile. Class II Reported terminated Distribution: Nationwide in the U.S.A [Official source for PHENOBARBITAL Sodium Injection, USP, 130 mg/mL, packaged as a) 25 x 1 mL Vials per box (NDC 42494...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0744-2022%22) ## Reasons in these listed records - Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile. These examples come from this result page and are not a ranking of every recall reason. ## Checking Vitae Enim Vitae Scientific, Inc. ### Is there a recall on vitae enim vitae scientific, inc. right now? This archive contains 4 records, including 0 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 Vitae Enim Vitae Scientific, Inc.](https://isitonrecall.com/check/?q=Vitae%20Enim%20Vitae%20Scientific%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)