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Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter
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Aug

04

  On July 28, 2017, ICU Medical has informed the US Food and Drug Administration (FDA) that they are issuing a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter identified as stainless steel within a single flexible container.

0.9% Sodium Chloride Injection from ICU Medical

NDC Number: 0409-7983-09

Lot Number: 61-841-FW

Expiration Date: January 01, 2018

Configuration/Count: 1000mL Single Dose Flexible Container

For additional information related to this recall, please visit the FDA Drug Recalls Page by clicking here.    

FDA Drug Recall, ICU Medical, ICU Medical has informed the US Food and Drug Administration (FDA) that they are issuing a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, Image, US Food and Drug Administration (FDA), Voluntary Nationwide Recall

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