Drug recall
Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper…
FDA recall event 85139 · Class III · CooperSurgical, Inc.
Key facts
| Event ID | 85139 |
|---|---|
| Recall numbers | Z-1713-2020 |
| Recalling firm | CooperSurgical, Inc. |
| Product type | Devices |
| Products | Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper Surgical Inc., (01) 2 0888937 021749 - Product Usage: Intended use of the product is the… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years. |
| Initiation date | Feb 28, 2020 |
| Report date | Apr 22, 2020 |
| Termination date | Aug 11, 2020 |
| City | Trumbull |
| State | CT |
| Country | United States |
| FEI number | 1216677 |
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: