FDA Drug Recalls

Recalls / Class II

Class IID-1415-2019

Product

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.

Affected lot / code info
All lots remaining within expiry.

Why it was 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.

Recalling firm

Firm
Premier Pharmacy Labs Inc
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
8265 Commercial Way, N/A, Weeki Wachee, Florida 34613-4511

Distribution

Quantity
2315 syringes
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2019-06-18
FDA classified
2019-06-21
Posted by FDA
2019-07-03
Terminated
2021-10-26
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1415-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls