---
title: "Fresenius Kabi Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Fresenius Kabi recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/fresenius-kabi/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Fresenius Kabi recall records

**0** reported ongoing

2 records in this archive. Latest source date Aug 11, 2026. 2 published notices do not supply a closure status.

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

Aug 11, 2026 FDA company announcement

### [Fresenius Kabi: Tyenne Injection 400 mg/20 mL vial](https://isitonrecall.com/recall/fdapress-1b670650d67911d9-fresenius-kabi-tyenne-injection-400-mg-20-ml-vial/)

Due to Presence of Glass Particles

Not supplied Published notice; closure not supplied

Distribution: Not supplied

[Official source for Fresenius Kabi: Tyenne Injection 400 mg/20 mL vial](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-nationwide-recall-tyenner-tocilizumab-aazg-injection-400-mg20-ml-vials-due)

Aug 5, 2026 FDA company announcement

### [Fresenius Kabi: Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL](https://isitonrecall.com/recall/fdapress-5b292dd0c8c4fbde-fresenius-kabi-morphine-sulfate-injection-usp-simplist-r-2-mg-1-ml/)

Due to a label mix-up

Not supplied Published notice; closure not supplied

Distribution: Not supplied

[Official source for Fresenius Kabi: Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-nationwide-recall-one-lot-morphine-sulfate-injection-usp-simplistr)

## Reasons in these listed records

- Due to Presence of Glass Particles
- Due to a label mix-up

These examples come from this result page and are not a ranking of every recall reason.

## Checking Fresenius Kabi

### Is there a recall on fresenius kabi right now?

This archive contains 2 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 Fresenius Kabi](https://isitonrecall.com/check/?q=Fresenius%20Kabi) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
