Drug recall
MiraLAX (Polyethylene Glycol 3350) Powder for Solution, Laxative, 17g/dose, 30 ONCE-DAILY DOSES, NET WT 17.9…
FDA recall event 56227 · Class III · Schering Corporation
Key facts
| Event ID | 56227 |
|---|---|
| Recall numbers | D-762-2010 |
| Recalling firm | Schering Corporation |
| Product type | Drugs |
| Products | MiraLAX (Polyethylene Glycol 3350) Powder for Solution, Laxative, 17g/dose, 30 ONCE-DAILY DOSES, NET WT 17.9 OZ (510g), OTC, Copyright & Distributed by : Schering-Plough HealthCare Products, Inc… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Defective Container: products may contain defective (burnt) cap liners and the product may have an off odor and off taste. |
| Initiation date | Jul 16, 2010 |
| Termination date | Nov 3, 2011 |
| City | Miami Lakes |
| State | FL |
| Country | United States |
| FEI number | 1010370 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports