Product Safety Recalls

Product Recall Tracker

Recall D-0403-2024

Description: fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL) 50 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0202-22, Bar code 70004020022,

Recall D-0403-2024 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberD-0403-2024
Event ID93456
DistributionNationwide in the USA
Quantity500 syringes
Recall ReasonLack of Assurance of Sterility
Drug ClassificationClass II
Drug Code Info20240403
Recall Initiation Date20231109
Report Date20240403
Classification Date20240322
Address755 Rainbow Rd Ste B
Windsor, CT 06095-1024
United States
Recalling FirmSCA Pharmaceuticals, LLC
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.