Product Safety Recalls

Product Recall Tracker

Recall D-0950-2022

Description: 8.4% Sodium Bicarbonate Injection, USP, 1 mEq/mL, 4.2 g/50 mL (84 mg/mL), 1 x 50 mL Pre-Filled Syringe, packaged in a) 10 x 1 syringe carton, b) 30 x 1 syringe carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-214-50

Recall D-0950-2022 Information

Mandated?Voluntary: Firm initiated
Recall NumberD-0950-2022
Event ID90211
DistributionNationwide in the USA
Quantity13612 syringes
Recall ReasonLack of Assurance of Sterility
Drug ClassificationClass II
Drug Code Info20220608
Recall Initiation Date20220518
Report Date20220608
Classification Date20220527
Address4500 12th Street Ext
West Columbia, SC 29172-3025
United States
Recalling FirmNephron Sterile Compounding Center LLC
Initial Notification Letter
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