Drug & medication recalls Moderate risk

Kroger Specialty Pharmacy, Inc. recalls Prolia 60 mg/1 mL PF syringe NDC 55513-0710-01 180 days supply.

Recall date
April 3, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
D-0748-2018
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

Prolia 60 mg/1 mL PF syringe NDC 55513-0710-01 180 days supply.

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.