Drug recall
Actimeta, Blister Packs
FDA recall event 68717 · Class II · GM Manufacturing Inc.
Key facts
| Event ID | 68717 |
|---|---|
| Recall numbers | F-2242-2014, F-2243-2014, F-2244-2014, F-2245-2014, F-2246-2014, F-2247-2014, F-2248-2014, F-2249-2014, F-2250-2014, F-2251-2014, F-2252-2014, F-2253-2014 and 34 more |
| Recalling firm | GM Manufacturing Inc. |
| Product type | Food |
| Products | Actimeta, Blister Packs, Actra-SX, Vinyl Bags, Adam, Blister Packs, Affirm XL, Blister Packs, Albert, Capsules and 41 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements. |
| Initiation date | Jul 3, 2014 |
| Report date | Aug 6, 2014 |
| Termination date | Sep 16, 2014 |
| City | Gardena |
| State | CA |
| Country | United States |
| FEI number | 3004256120 |
At a glance
- 10–99 Products in this recall
- 1–9 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 · Source date: