Fresenius Kabi USA, LLC recalls
2 notices naming Fresenius Kabi USA, LLC in the last 60 days, newest first. The name is the one FDA gives to the recalling firm.
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Hazard and remedy text is quoted from the agency, unedited. The red tag names the kind of risk with a word from that text. Every notice links to its official page.
Fresenius Kabi USA, LLC: Tyenne
Hazard (FDA): Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
FDAMedicines
Quality defect
Fresenius Kabi USA, LLC: Morphine Sulfate Injection
Hazard (FDA): Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
FDAMedicines
For recalls older than this period, search U.S. Food and Drug Administration (opens in a new tab).
Questions about Fresenius Kabi USA, LLC recalls
How many Fresenius Kabi USA, LLC recalls are listed?
2 notices naming Fresenius Kabi USA, LLC were published by FDA in the 60 days before October 3, 2026, in: medicines. Older recalls of the firm are on the site of the agency.
What is the most recent Fresenius Kabi USA, LLC recall?
“Fresenius Kabi USA, LLC: Tyenne”, published on September 2, 2026. FDA describes the hazard as: “Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.”
I own a Fresenius Kabi USA, LLC product. Is it recalled?
Only if it matches the model, lot or date codes on one of the notices. Open the notice and compare the codes with the ones printed on your product; the brand alone is not enough.
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