[Recalled] Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the volumetric delivery of fluids used in Enteral applications. — The firm is adding an add
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the volumetric delivery of fluids used in Enteral applications. |
|---|---|
| Brand / manufacturer | MOOG Medical Devices Group |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0764-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 12 October 2012 |
| EAN / barcode | 105068015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The firm is adding an addendum to the operator's manual for Infinity Enteralite Ambulatory Feeding Pumps pertaining to the Infinite Dose mode and the inability of the Pump to detect air in line.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from MOOG Medical Devices Group
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.