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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Vet
Medical Devices/Home Healthcare

Hospira Inc.: Plum A+ Infusion Pumps Recalled for Potential Alarms and Therapy Interruption

Agency Publication Date: July 16, 2014
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Summary

Hospira Inc. is recalling 467 units of the Plum A+ Infusion System because a component called the fluid shield diaphragm may be out of specification. This defect can cause the pump to trigger 'Door Open while pumping' (N250) or 'Unrecognizable Cassette' (N100) alarms during setup or infusion. These alarms can lead to an unexpected delay or interruption in the delivery of critical fluids, such as medications, nutrients, or blood, to patients.

Risk

If the fluid shield diaphragm fails, it triggers audible and visual alarms that stop the infusion process. This interruption can result in a delay of therapy, which may have serious health consequences depending on the patient's condition and the medication being delivered.

What You Should Do

  1. Check your Plum A+ Infusion System (List Number 60529) to see if its serial number matches any of the 467 affected units. Affected serial numbers include 14315003, 14315004, 14315011, 14315019, 14315048, 14315100, 14315200, 14315300, 14315400, 14315491, and others listed in the affected products section.
  2. If your device is identified as one of the affected units, immediately contact your healthcare provider or the manufacturer to report the issue and receive guidance on the next steps.
  3. Pay close attention to any N250 'Door Open' or N100 'Unrecognizable Cassette' alarms that occur during pump setup, infusion, or testing, as these indicate the defect is present.
  4. Contact Hospira Inc. (now ICU Medical Inc.) for technical support and to arrange for any necessary equipment inspections or repairs.
  5. For additional information or questions regarding this recall, contact the FDA’s Center for Veterinary Medicine or the manufacturer directly.

Your Remedy Options

📋Other Action

Equipment inspection and potential repair

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Plum A+ Infusion System
Model:
List Number: 60529
Lot Numbers (467):
14315003
14315004
14315005
14315008
14315009
14315011
14315012
14315013
14315014
14315015
14315017
14315018
14315019
14315020
14315022
14315023
14315025
14315026
14315027
14315028
14315029
14315030
14315031
14315034
14315035
14315036
14315037
14315038
14315040
14315041
14315043
14315044
14315045
14315046
14315047
14315048
14315049
14315050
14315051
14315052
14315053
14315054
14315055
14315056
14315057
14315058
14315059
14315061
14315062
14315063

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 67761
Status: Resolved
Manufacturer: Hospira Inc.
Sold By: Hospira Inc.; ICU Medical Inc
Manufactured In: United States
Units Affected: 467 pumps
Distributed To: Alabama, Colorado, Florida, Iowa, Idaho, Illinois, Indiana, Kansas, Louisiana, Minnesota, Missouri, North Carolina, New York, Oklahoma, Pennsylvania, Tennessee, Texas, Virginia, District of Columbia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response