HIGH
FDA DRUG
Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-696-02 (vial), NDC 63323-696-25 (carton)
EPINEPHRINE
Failed Impurities/Degradations
Brand hub
Fresenius Kabi USA, LLC Recalls
12 recalls found for Fresenius Kabi USA, LLC. Check current safety alerts and related brands before using affected products.
- Active recalls
- 12
- Pages
- 1
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recall for Sterility Concerns (2026) Affecting US Nationwide, R
Lack of Assurance of Sterility
DEXTROSE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP, 0.9% (900 mg per 100 mL) (9 mg per mL) 100 mL in a 100 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 600047, Unit of Use...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 mL in a 500 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC:...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC:...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recall Active Over Sterility Assurance Issue (2026)
Lack of Assurance of Sterility
DEXTROSE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
DEXTROSE
Lack of
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL) 500 mL in a Single Dose freeflex bag, 500 mL x 20, Manufactured for: Fresenius Kabi USA, LLC ("Fresenius Kabi"), IL 60047, Unit of...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi Famotidine Injection Recall Expands for Microbial Contamination in 2.2 Million Vials
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Famotidine
Microbial Contamination
Brand Statistics
Total Recalls
12
Pages
1