Sodium Bicarbonate INJ 8 recalled over sterility concerns
- Recall date
- June 18, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Premier Pharmacy Labs Inc recalls Sodium Bicarbonate INJ 8.4%, 50 mEq/50mL (84mg/mL) (1mEq/mL), 50mL Sterile SDV, Rx only, Premier Pharmacy Labs, 8265 Co…
- Recall number
- D-1426-2019
- FDA classification
- Class II
- Brand / firm
- Premier Pharmacy Labs Inc
- Sold / distributed
- Nationwide in the USA
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Sodium Bicarbonate INJ 8.4%, 50 mEq/50mL (84mg/mL) (1mEq/mL), 50mL Sterile SDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-232-39, barcode 8 69623 23239 3.
Get recall alerts
Free email alert whenever Premier Pharmacy Labs Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Premier Pharmacy Labs Inc