Devices

Device Recall Hospira Midlength Secondary I.V. Set

Model / Serial
Lot numbers: 530764W, 530774W, 540464W, 550484W, 550494W, 560924W, 561334W, 570494W, 570984W, 570994W, 580014W, 590834W, 591134W, 611004W, 611014W, 611364W, 611374W, and 620554W.
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
Latex-free. Midlength Secondary I.V. Set, convertible pin, 40 inch with extension hook for use with OMNI-FLOW Medication Management System and PLUM Series Infusions Systems, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 1139-48.
Manufacturer
Hospira Inc.
1 Event
- Recall of Device Recall Hospira Midlength Secondary I.V. 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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