Nestle Healthcare Nutrition, Inc.
Country not established
- Devices
- 13
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Nestle Healthcare Nutrition, Inc. makes
Nestlé Healthcare Nutrition, Inc. manufactures enteral delivery pump sets, designed for administering liquid nutritional formulations directly into the gastrointestinal tract. These devices are intended for use in clinical settings where patients require controlled, continuous feeding support.
The company’s enteral delivery pump sets are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These products are registered with the U.S. Food and Drug Administration, adhering to federal medical device compliance standards.
Catalogue
Search and filter all 13 devicesCompany details
- DUNS number
- 829712640
- [email protected]
- Phone
- 1-877-338-4238
FDA recalls
FDA recall records list 1 recall initiated by Nestle Healthcare Nutrition, Inc., initiated on 2013-07-24. By recorded status: 1 terminated. The reasons filed fall into these groups: labeling or instructions for use, sterility or contamination and packaging. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2013
- 24 Jul 2013 Z-1922-2013 Class II Terminated Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat NG Tubes because they have been delivered in an insufficiently sealed pouch, thus compromising the sterility claimed on the label.
Full distribution text
- 24 Jul 2013 Z-1922-2013 Class II Terminated Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat NG Tubes because they have been delivered in an insufficiently sealed pouch, thus compromising the sterility claimed on the label.
Frequently asked questions
How many devices does Nestle Healthcare Nutrition, Inc. have in the registry?
The registry currently lists 13 devices for Nestle Healthcare Nutrition, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nestle Healthcare Nutrition, Inc.'s devices?
Among its 13 most recently registered devices, Nestle Healthcare Nutrition, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Nestle Healthcare Nutrition, Inc.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Nestle Healthcare Nutrition, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Nestle Healthcare Nutrition, Inc.?
FDA recall records list 1 recall initiated by Nestle Healthcare Nutrition, Inc., the most recent initiated on 24 Jul 2013. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Nestle Healthcare Nutrition, Inc. in the registry?
The most recently registered devices listed for Nestle Healthcare Nutrition, Inc. include COMPAT® 08742000, COMPAT® 12262825, COMPAT® 08742400 and COMPAT® 08741800.