The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error.
Reason for recall: The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error. Distribution: US Nationwide distribution in the states of CA, NV, NY. Quantity: 3 Boxes (25 per box, 75 total units) Lot/code info: UDI-DI: 20612479170302;
20612479170302
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.