Drug recall
5LK7 / 20000 IU/KG VIT D3 (Weight VARIES)
FDA recall event 62479 · Class I · PMI Nutrition International
Key facts
| Event ID | 62479 |
|---|---|
| Recall numbers | V-007-2015, V-008-2015, V-009-2015, V-010-2015, V-011-2015, V-012-2015, V-013-2015, V-014-2015, V-015-2015, V-016-2015, V-017-2015, V-018-2015 and 110 more |
| Recalling firm | PMI Nutrition International |
| Product type | Veterinary |
| Products | 5LK7 / 20000 IU/KG VIT D3 (Weight VARIES), AQUAMAX CUSTOM 41/12 1/8 50 LB, AQUAMAX CUSTOM 41/12 3/16 50 LB, AQUAMAX DENSE 4000 50 LB, AQUAMAX FINGERLING 300 50 LB and 108 more |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Four customer complaints received. One customer reported mortality of 7 parakeets and one customer reported mortality of 14 small birds. Veterinarian diagnosis on two of the complaints indicated…, Four customer complaints received. One customer reported mortality of 7 parakeets and one customer reported mortality of 14 small birds. Veterinarian diagnosis on two of the complaints indicated…, Four… |
| Initiation date | Jul 3, 2012 |
| Report date | Oct 15, 2014 |
| Termination date | Oct 9, 2014 |
| City | Richmond |
| State | IN |
| Country | United States |
| FEI number | 1819617 |
At a glance
- 100–999 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: