Devices

Device Recall Deltec 3000 Large Volume Infusion Pump,

Model / Serial
All serial numbered devices affected.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
AL, AR, AZ, CA, CO, CT, DC, FL. GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, ,MO, MS, MT, NC, ND, NE,NH, NJ, NM, NV, NY, OH, OK OR,PA, RI,SC, TN, TX, UT,VA, VT, WA, WI, WV, and WY
Product Description
Deltec¿ 3000 Large Volume Infusion Pump, CE 0473, RX Only, Smiths Medical MD, Inc. 1265 Grey Fox Road, St. Paul, MN 55112, USA, Made in UK. || Reorder numbers 21-5301-01 & 21-5306-01 || The product is used for general drug delivery infusion therapies. The product is only intended to be used by trained clinicians.
Manufacturer
Smiths Medical MD, Inc.
1 Event
- Recall of Device Recall Deltec 3000 Large Volume Infusion Pump,

Manufacturer

Smiths Medical MD, Inc.

Manufacturer Address
Smiths Medical MD, Inc., 1265 Grey Fox Rd, Saint Paul MN 55112-6929
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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