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
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
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Health & Personal Care
HIGH
FDA DRUG
BD and Fresenius Kabi 1,000 mL Sodium Chloride Injection Recall for Sterility Concerns (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DEVICE
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen...
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
ARROW INTERNATIONAL
Due to
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, Distributed by BD, Manufactured by Fresenius Kabi USA, LLC ("Fresenius...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DEVICE
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14433
Windstone Medical Packaging
The product
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
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance
Fresenius Kabi USA recalls 0.9% Sodium Chloride Injection units distributed nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers should stop use and contact Fresenius Kabi for guidance.
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 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 5% Dextrose Injection Recall for Sterility Concerns (2026) Affecting US Nationwide, R
Lack of Assurance of Sterility
DEXTROSE
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
Food & Beverages
HIGH
FDA FOOD
Lone Star Dairy Products Recalls 1.79M Lbs Spray Dried Dairy Powder Over Salmonella Risk (2026)
Salmonella spp. identified in finished product testing
Lone Star Dairy Products
Salmonella spp.
HIGH
FDA DEVICE
ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF ASK-45703-MGH UDI...
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
ARROW INTERNATIONAL
Due to
HIGH
FDA DEVICE
Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is intended for injection or aspiration of fluids. The needle...
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
ARROW INTERNATIONAL
Due to
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, 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 DEVICE
FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arrow Epidural...
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
ARROW INTERNATIONAL
Due to
HIGH
FDA DEVICE
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994A
Windstone Medical Packaging
The product
HIGH
FDA DEVICE
PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous...
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
ARROW INTERNATIONAL
Due to
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