The Recall Desk

FDA (Drugs) recall action 71681

Hospira Inc. recalled 2 products on 2015-07-22

The FDA (Drugs) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2015-07-22
Critical
0
Units
—

Why these products were recalled

Crystallization; identified as calcium salt of Ketorolac

The agency’s own wording, quoted from the enforcement report.

States named across these recalls

1–2 of 2