PlainRecalls
FDA Drug Moderate Class II Terminated

Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-185-10, barcode 0 69623 18510 5.

Reported: July 3, 2019 Initiated: June 18, 2019 #D-1415-2019

Product Description

Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-185-10, barcode 0 69623 18510 5.

Reason for Recall

Lack of Assurance of Sterility: FDA inspection found insufficient environmental controls, potential cross contamination and lack of product specific process validations that can result in a lack of sterility assurance.

Details

Recalling Firm
Premier Pharmacy Labs Inc
Units Affected
2315 syringes
Distribution
Nationwide in the USA
Location
Weeki Wachee, FL

Frequently Asked Questions

What product was recalled?
Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-185-10, barcode 0 69623 18510 5.. Recalled by Premier Pharmacy Labs Inc. Units affected: 2315 syringes.
Why was this product recalled?
Lack of Assurance of Sterility: FDA inspection found insufficient environmental controls, potential cross contamination and lack of product specific process validations that can result in a lack of sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 3, 2019. Severity: Moderate. Recall number: D-1415-2019.