Drug recall
Tylenol Acetaminophen Extended Release Arthritis Pain, for the temporary relief of minor arthritis pain…
FDA recall event 31517 · Class III · Select Distributors, Inc
Key facts
| Event ID | 31517 |
|---|---|
| Recall numbers | D-225-5 |
| Recalling firm | Select Distributors, Inc |
| Product type | Drugs |
| Products | Tylenol Acetaminophen Extended Release Arthritis Pain, for the temporary relief of minor arthritis pain. Retail carton dispenser: Acetaminophen 250 mg, Retail individual pouch: Acetaminophen 650 mg… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeling: Retail dispensing carton indicates wrong strength of Acetaminophen but retail pouches are labled with proper strength. |
| Initiation date | Feb 28, 2005 |
| Termination date | Apr 1, 2008 |
| City | Dallas |
| State | TX |
| Country | United States |
| FEI number | 3003727136 |
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