Devices

Device Recall LifeShield I.V. Pump Set

Model / Serial
Lot numbers: 521815H, 571015H, and 571615H.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- U.S., Puerto Rico, Dominican Republic, Bahamas, Virgin Islands, Argentina, Australia, Bahrain, Belgium, Canada, China, Denmark, Ecuador, EI Salvador, Finland, France, Germany, Greece, Guatemala, Hong Kong, Ireland, Italy, Jordan, Kuwait, Lebanon, Libya, Mexico, Netherlands, New Zealand, Nicaragua, Norway, Oman, Panama, Peru, Philippines, Poland, Portugal, San Marino, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Kingdom, Uruguay, and United Arab Emirates.
Product Description
Lifeshield, latex-free, Primary I.V. Pump Set with Distal Microbore Patient Line and Gravity Flow Prevention Valve, convertible pin, 110 inch with high-pressure filter, orange polyethylene-lined/light resistant tubing and OPTION-LOK for use with OMNI-FLOW infusion system, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 12163-01.
Manufacturer
Hospira Inc.
1 Event
- Recall of Device Recall LifeShield I.V. Pump Set

Manufacturer

Hospira Inc.

Manufacturer Address
Hospira Inc., 375 N Field Dr, Lake Forest IL 60045-2513
Manufacturer Parent Company (2017)
Pfizer
Source
USFDA

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