Tag Archives: zero defects

Recall of Sodium Acetate Injection Due to the Presence of Particulate Matter

Fresenius Kabi is a global health care company that produces and specializes in medication and infusion/transfusion technology. Fresenius Kabi USA voluntarily recalled seven lots of Sodium Acetate Injection on Monday, March 7th. Various amounts of iron, sodium, silicon, chromium, aluminum and cellulose found in these injections led to seven lots being recalled. The presence of…
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Serialization Challenges of Track & Trace in the Biopharma Industry

10% of drugs sold around the world are fake.  Counterfeit medicines are the cause of on average 1 million deaths yearly.  Increasing of online purchases and disrupted supply chains have intensified and made the risk of counterfeit medicines due to COVID-19. Drugs are “tracked” once after the product has left the manufacturer and landed where…
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Sagent Pharmaceuticals, Inc. Issues Nationwide Recall

November 19, 2021, Sagent Pharma announces a voluntary nationwide recall of Levetiracetam Injection.  Four lots of Levetiracetam was recalled due to the lack of a sterile product.  Issues pertaining to container closure integrity was brought to attention when found in reserve sample vials.  Sagent Pharmaceuticals did not follow USP suggested guidelines for container closure integrity—distributing…
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ICU Medical, Inc. Amino Acid Injection Recall

Particulate matter was found in an Amino Acid Injection in September.  ICU Medical, Inc. voluntarily recalled one lot of Aminosyn II, 15% of 2,112 units.  This is a Sulfite Free IV solution used in hospitals.  The recall was enforced due to particles such as fibers, hairs and proteinaceous materials.  These particles were found when ICU…
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