Drug recall
Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt…
FDA recall event 62471 · Class II · Maquet Inc.
Key facts
| Event ID | 62471 |
|---|---|
| Recall numbers | Z-2210-2012 |
| Recalling firm | Maquet Inc. |
| Product type | Devices |
| Products | Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222 932-1888 [email protected] www.maquet.com Used to… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip. |
| Initiation date | May 29, 2012 |
| Report date | Aug 22, 2012 |
| Termination date | Apr 3, 2014 |
| City | Wayne |
| State | NJ |
| Country | United States |
| FEI number | 3001451475 |
At a glance
- 1–9 Products in this recall
- None 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: