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Braun Medical Inc. is recalling two lots of 0.9% Sodium Chloride for Injection USP 1000 mL E3 containers. This voluntary recall affects products distributed in the United States and is due to ...
Heparin Sodium in Sodium Chloride Injection is used as an anticoagulant to maintain catheter patency. The affected product is packaged in 2,000 USP units per 1,000 mL, contained in VIAFLEX Plus ...
B. Braun Medical Inc. (B. Braun), is voluntarily recalling two (2) lots of 0.9% Sodium Chloride for Injection USP 1000 mL in E3 containers within the United States to the consumer level.
(RTTNews) - Dr. Reddy's Laboratories Ltd. is recalling select Levetiracetam in Sodium Chloride Injection in the United States citing mislabeling of infusion bag, according to the U.S. Food and ...
Baxter International Inc. (NYSE:BAX) is voluntarily recalling one lot of Heparin Sodium in 0.9% Sodium Chloride Injection to the consumer level due to the potential for elevated endotoxin levels ...
Product Overwrap Description - Levetiracetam in 0.75% Sodium Chloride Injection (1,000 mg/100 mL) (Photo: Business Wire) Product Infusion Bag Primary Description with ...
At Baxter’s North Cove site, here are the medications and their NDCs: Brevibloc premix sodium chloride injection solution 10Mg/Ml 250 Ml X10 — 10019-0055-61 Brevibloc premix injection 2000 Mg ...
Am J Health Syst Pharm. 2005;62(23):2410-2412. To increase the flexibility in preparation time and storage and decrease waste after reconstituting pantoprazole sodium for injection, it would be ...
Dr. Reddy’s (RDY) Laboratories announced that it is recalling one Batch/Lot No: A1540076 of Levetiracetam in 0.75% Sodium Chloride Injection, 1,000 mg/100 mL single-dose infusion bags to the ...
At this time, the Company has not received any reports of adverse events related to this recall. Baxter International is recalling 1 lot of Heparin Sodium in 0.9% Sodium Chloride Injection due to ...
The stability of treprostinil sodium after dilution in three common i.v. infusion vehicles was assessed. The chemical stability of treprostinil sodium was tested over a 48-hour period at 40 °C ...
The product is being recalled because the infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL single-dose bag, while the aluminum overwrap ...
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