Kroger Specialty Pharmacy, Inc. recalls Humira Pen Sub-q Kit a.) 40 mg/0.8 mL (NDC 00074-4339-02); Humira Pen Psor Kit b.) 40 mg/0.8 mL (NDC 00074-4339-07) 28…
- Recall date
- April 3, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0734-2018
- FDA classification
- Class II
- Brand / firm
- Kroger Specialty Pharmacy, Inc.
- Sold / distributed
- MS, LA, AR, IL, FL
Why it was recalled
Lack of Processing Controls.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Humira Pen Sub-q Kit a.) 40 mg/0.8 mL (NDC 00074-4339-02); Humira Pen Psor Kit b.) 40 mg/0.8 mL (NDC 00074-4339-07) 28 day supply, Rx Only,
Get recall alerts
Free email alert whenever Kroger Specialty Pharmacy, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Kroger Specialty Pharmacy, Inc.