The Plum A+ Infusion System is designed to meet the fluid delivery… — Class I medical device recall Z-1073-2015
Terminated recall by Hospira Inc., reported 2015-03-04, distributed in AK, AL, AR, CA, CO, CT, DC, DE…. One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels
| Recall number | Z-1073-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2014-07-02 |
| Classified | 2015-02-23 |
| Reported by FDA | 2015-03-04 |
| Terminated | 2017-05-24 |
| Distributed | AK, AL, AR, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
| Countries outside the US | AE, BR, CA, CO, EC, ES, FR, GB, IL, IT, MX, OM, PE, SA, TR, VE |
| Quantity | 4,656 infusion |
| Reason classes | device malfunction |
| Serial numbers | 15445226, 15446166, 15446197, 15446876, 15446886, 15447262, 15447455, 15447612, 15447652, 15448232, 15448292, 15448296, 15448362, 15448426, 15450782, 15451773, 15541171, 15541871, 15542831, 15542861, 15542891, 15542911, 15542921, 15543011, 15543031 and 475 more |
Product
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environments. It is a cassette based multi-function infusion system. The Plum A+ allows two lines in and one line out. The pump can be used for standard, piggyback, or concurrent delivery. Therapy modes include: Standard Infusions, Multistep Programming, Loading Dose, and Dose Calculation. The Plum A+ is designed to deliver parenteral, enteral, or epidural infusions over a broad range of infusion rates from multiple fluid container types. Each system includes a pumping module and an assortment of disposable IV sets, optional accessories, and an operator's manual.
Reason for recall
One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1073-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.