Hospira Plum 360 Infusion Pump Recall [Canada]


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Canada/Ottawa: Hospira Plum 360 Infusion Pump Recall [Canada]Health Canada recalls certain batch/lots of Hospira Plum 360 Infusion Pumps running device software version 15.02 due to suspected operational failure and consequential interruption of any ongoing therapy and patient injury hazards. HCSC: http://ht.ly/NFHE307VXai

Direct link: http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/61738r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Infusion Pumps are subject to this recall:

  • Hospira Plum 360 Infusion Pumps, model number 30010 running software version 15.02

Please consult the photograph above for details of the product’s packaging, design and retail presentation.

==> No barcodes, UPCs, item numbers or other identification numbers were listed with this recall notification.

According to Health Canada, when the AC power is lost and quickly resumed, the recalled Infusion Pump software incorrectly classifies the event as an “e323 alarm” condition resulting in an interruption of any ongoing therapy. If this defect occurs, the Infusion Pump requires manual user input to resume previous infusion and patient therapy.

If you believe you have purchased or have in your possession any of the recalled Infusion Pumps, please use another model or brand of Infusion Pump until this matter is resolved. If this is not possible, immediately contact Hospira Inc. for repair details.

If you have any questions about this recall notification, please contact Hospira Global Complaint Management at 1-800-241-4002 from 9:00 AM to 5:00 PM, Eastern Standard Time, Monday to Friday. Alternatively, you can e-mail the company at supportservices@hospira.com.

Please note: the Canada Consumer Product Safety Act prohibits recalled products from being redistributed, sold or even given away in Canada.

==> To see all recalls and notifications relating to Medical Devices, please search for “medical” using the Search Box at the top of this page.

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More information about this recall:
HCSC ID number: RA-61738
Recalls Direct RIN: 8116-2017

Want to read more about this recall?
==> Please click on the links above to visit the originating site.
Want to read more about other recalls?
==> Please click on the links below.

General information:
More recalls? Back to the main Recalls Direct page:
==> http://www.RecallsDirect.com/
About the Recalls Direct service:
==> http://wp.me/P2bVty-2
Visit the Living Safely site:
==> http://www.LivingSafely.org/
Report an unsafe product you purchased in Canada [external: new window opens]:
==> http://www.hc-sc.gc.ca/cps-spc/advisories-avis/incident/index-eng.php
Search for a recalled product on the Health Canada Web site [external: new window opens]:
==> http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/index-eng.php

We welcome your feedback:
Want to e-mail or share this recall?
==> Simply use the “Share this” options below.
Is this recall relevant to you? Please let us know!
==> Click on the “Like” button below.
E. & O. E.

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