Drug recall
Tebamide Suppositories, (Trimethobenzamide HCl) 100 mg, Pediatric Suppositories, 10 count boxes, Rx Only, For…
FDA recall event 28406 · Class III · G & W Labs Inc
Key facts
| Event ID | 28406 |
|---|---|
| Recall numbers | D-132-4 |
| Recalling firm | G & W Labs Inc |
| Product type | Drugs |
| Products | Tebamide Suppositories, (Trimethobenzamide HCl) 100 mg, Pediatric Suppositories, 10 count boxes, Rx Only, For Rectal Administration, G&W Laboratories, South Plainfield, NJ ----- NDC 0713-0107-09 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent; benzocaine (stability) |
| Initiation date | Feb 25, 2004 |
| Termination date | Jun 28, 2004 |
| City | South Plainfield |
| Country | United States |
| FEI number | 2210277 |
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