Drug recall
Povidone Iodine Prep Pads (Povidone Iodine, USP, 10%), Antiseptic/Germicide, For Hospital and Professional Use…
FDA recall event 58311 · Class I, Class II · H & P Industries, Inc.
Key facts
| Event ID | 58311 |
|---|---|
| Recall numbers | D-533-2011, D-534-2011 |
| Recalling firm | H & P Industries, Inc. |
| Product type | Drugs |
| Products | Povidone Iodine Prep Pads (Povidone Iodine, USP, 10%), Antiseptic/Germicide, For Hospital and Professional Use Only, Uses: First aid to help prevent infection in minor cuts, scrapes, and burns…, Povidone Iodine Prep Pads, (Povidone Iodine, USP 10%), Use: First aid to help prevent infection in minor cuts, scrapes, and burns. Labeled under the following names: a) Povidone Iodine Prep Pad (10%… |
| Classification | Class I, Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Microbial Contamination of Non-Sterile Products: The recall of all lots of Povidine Iodine Prep Pads was initiated due to results of analytical testing showing the presence of objectionable organisms… |
| Initiation date | Mar 15, 2011 |
| Termination date | Aug 1, 2012 |
| City | Hartland |
| State | WI |
| Country | United States |
| FEI number | 2128643 |
At a glance
- 1–9 Products in this recall
- None 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