Drug recall
Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758
FDA recall event 83681 · Class II · Philips North America LLC
Key facts
| Event ID | 83681 |
|---|---|
| Recall numbers | Z-2549-2019 |
| Recalling firm | Philips North America LLC |
| Product type | Devices |
| Products | Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The recall is being initiated due to incorrect age range labeling (8+ yrs) on the foil packaging for infant/child pad cartridges. The infant/child pad cartridge is designed for use with the… |
| Initiation date | Aug 8, 2018 |
| Report date | Oct 2, 2019 |
| Termination date | Apr 29, 2021 |
| City | Bothell |
| State | WA |
| Country | United States |
| FEI number | 1000524572 |
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: