Drug recall
1) Pivetal Hypodermic Needle, Polypropylene Hub, REF 21295175, 25G X 5/8", regular bevel, rigid pack, single…
FDA recall event 88747 · Class II · Medline Industries Inc
Key facts
| Event ID | 88747 |
|---|---|
| Recall numbers | V-0001-2022 |
| Recalling firm | Medline Industries Inc |
| Product type | Veterinary |
| Products | 1) Pivetal Hypodermic Needle, Polypropylene Hub, REF 21295175, 25G X 5/8", regular bevel, rigid pack, single use only, Rx only, Veterinary use only; 2) Pivetal Hypodermic Needle, Polypropylene Hub… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Pinholes found in the needle cap which could compromise sterility. |
| Initiation date | Sep 15, 2021 |
| Report date | Oct 27, 2021 |
| Termination date | Mar 23, 2023 |
| City | Northfield |
| State | IL |
| Country | United States |
| FEI number | 1417592 |
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 · Source date: