--- title: "Medicina Uk Ltd Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medicina Uk Ltd recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/medicina-uk-ltd/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medicina Uk Ltd recall records **8** reported ongoing 8 records in this archive. Latest source date Jul 4, 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 Jul 4, 2022 FDA device enforcement ### [Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD](https://isitonrecall.com/recall/fda-device-z-0107-2023-medicina-enfit-1ml-reusable-low-dose-enteral-syringe-code-lhe01ld/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0107-2023%22) Jul 4, 2022 FDA device enforcement ### [Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05](https://isitonrecall.com/recall/fda-device-z-0108-2023-medicina-enfit-5ml-reusable-enteral-syringe-code-lhe05/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0108-2023%22) Jul 4, 2022 FDA device enforcement ### [Medicina Oral Tip Syringe 0.5ml Code: OT005](https://isitonrecall.com/recall/fda-device-z-0109-2023-medicina-oral-tip-syringe-0-5ml-code-ot005/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina Oral Tip Syringe 0.5ml Code: OT005](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0109-2023%22) Jul 4, 2022 FDA device enforcement ### [Medicina Oral Tip Syringe 1ml Code: OT01](https://isitonrecall.com/recall/fda-device-z-0110-2023-medicina-oral-tip-syringe-1ml-code-ot01/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina Oral Tip Syringe 1ml Code: OT01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0110-2023%22) Jul 4, 2022 FDA device enforcement ### [Medicina Oral Tip Syringe 2.5ml Code: OT25](https://isitonrecall.com/recall/fda-device-z-0111-2023-medicina-oral-tip-syringe-2-5ml-code-ot25/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina Oral Tip Syringe 2.5ml Code: OT25](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0111-2023%22) Jul 4, 2022 FDA device enforcement ### [Medicina Reusable Oral syringe 1ml Code: OTH01](https://isitonrecall.com/recall/fda-device-z-0112-2023-medicina-reusable-oral-syringe-1ml-code-oth01/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina Reusable Oral syringe 1ml Code: OTH01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0112-2023%22) Jul 4, 2022 FDA device enforcement ### [Medicina Reusable Oral syringe 5ml Code: OTH05](https://isitonrecall.com/recall/fda-device-z-0113-2023-medicina-reusable-oral-syringe-5ml-code-oth05/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina Reusable Oral syringe 5ml Code: OTH05](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0113-2023%22) Jul 4, 2022 FDA device enforcement ### [Medicina Reusable Oral syringe 2.5ml Code: OTH25](https://isitonrecall.com/recall/fda-device-z-0114-2023-medicina-reusable-oral-syringe-2-5ml-code-oth25/) Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification Class II Reported ongoing Distribution: Nationwide [Official source for Medicina Reusable Oral syringe 2.5ml Code: OTH25](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0114-2023%22) ## Reasons in these listed records - Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification These examples come from this result page and are not a ranking of every recall reason. ## Checking Medicina Uk Ltd ### Is there a recall on medicina uk ltd 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 Medicina Uk Ltd](https://isitonrecall.com/check/?q=Medicina%20Uk%20Ltd) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)