Drug recall
Vicodin HP Tablets, (hydrocodone bitartrate and acetaminophen, USP), 10mg / 660mg, 100 count bottles, Rx only…
FDA recall event 27595 · Class III · Amerisource Health Services Corp
Key facts
| Event ID | 27595 |
|---|---|
| Recall numbers | D-070-4 |
| Recalling firm | Amerisource Health Services Corp |
| Product type | Drugs |
| Products | Vicodin HP Tablets, (hydrocodone bitartrate and acetaminophen, USP), 10mg / 660mg, 100 count bottles, Rx only, Mfg by: Abbott Laboratories, North Chicago, IL 60064, Pkg by: American Health Packaging… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeling: Extended expiration date-product incorrectly declares expiration date as 6/2006 rather than the correct date of 6/2005(by manufacturer) |
| Initiation date | Oct 29, 2003 |
| Termination date | Feb 12, 2004 |
| City | Columbus |
| Country | United States |
| FEI number | 3000209995 |
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