Drug recall
Puritan Bennett Cuff Pressure Manager, REF: 180-03
FDA recall event 92941 · Class II · Covidien
Key facts
| Event ID | 92941 |
|---|---|
| Recall numbers | Z-2651-2023 |
| Recalling firm | Covidien |
| Product type | Devices |
| Products | Puritan Bennett Cuff Pressure Manager, REF: 180-03 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Inadequate internal fixation of the power inlet port to the cuff pressure manager device causes the external power inlet to became dislodged within the device housing after several uses, which… |
| Initiation date | Aug 22, 2023 |
| Report date | Oct 11, 2023 |
| City | Boulder |
| State | CO |
| Country | United States |
| FEI number | 2936999 |
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: