Drug recall
Metrix 12Gauge Donor Set, Part # 5350, non-sterile, not for human use, packed in 25 per polybag, 200 units per…
FDA recall event 74592 · Class II · The Metrix Company
Key facts
| Event ID | 74592 |
|---|---|
| Recall numbers | V-0017-2017, V-0018-2017, V-0019-2017, V-0020-2017, V-0021-2017, V-0022-2017, V-0023-2017, V-0024-2017, V-0025-2017, V-0026-2017, V-0027-2017 |
| Recalling firm | The Metrix Company |
| Product type | Veterinary |
| Products | Metrix 12Gauge Donor Set, Part # 5350, non-sterile, not for human use, packed in 25 per polybag, 200 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002., Metrix 1L Defibro Bag, Part # 2560, non-sterile, not for human use, packed in 60 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002., Metrix 1L Defibro Bag, Part # 4770, non-sterile, not for human use, packed in 60 units per case. The responsible firm name on the label is The Metrix Company, Dubuque, IA 52002., Metrix 2L Blood Donor Bag with Needle, Part # 7310, non-sterile, not for human use, packed individually in polybags, 100 units per case. The responsible firm name on the label is The Metrix Company…, Metrix 600ML Blood Donor Bag, Part # 7070, non-sterile, not for human use, packed individually in polybags, 125 units per case. The responsible firm name on the label is The Metrix Company, Dubuque… and 6 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The hub of the needle on affected products may contain aluminum flakes. |
| Initiation date | Jul 7, 2016 |
| Report date | Nov 30, 2016 |
| Termination date | Oct 16, 2017 |
| City | Dubuque |
| State | IA |
| Country | United States |
| FEI number | 1000117446 |
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: