Reported Jul 16, 2014 · Terminated

GemStar infusion pump, List numbers 13000 and 13100, GemStar Infusion Pump (pain management) List number 13150. Used…

Hospira Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579

Is this the product you have?

  • GemStar infusion pump, List numbers 13000 and 13100, GemStar Infusion Pump (pain management) List number 13150. Used for intravenous, arterial, subcutaneous, short-term epidural infusion and parenteral administration of general I.V. fluids, medications, nutritional fluids, and blood/blood products.
Lot codes and dates
  • 1)
  • List Number13000
  • Serial Numbers

    2,714 of 2,714 codes

    • 9221423
    • 12470045
    • 12470063
    • 12470085
    • 12470109
    • 12470130
    • 12470133
    • 12470135
    • 12470138
    • 12470144
    • 12470145
    • 12470147
    • 12470152
    • 12470153
    • 12470154
    • 12470156
    • 12470157
    • 12470158
    • 12470160
    • 12470162
    • 12470163
    • 12470164
    • 12470165
    • 12470167
    • 12470168
    • 12470169
    • 12470171
    • 12470172
    • 12470173
    • 12470174
    • 12470177
    • 12470180
    • 12470207
    • 12470208
    • 12470209
    • 12470220
    • 12470225
    • 12470239
    • 12470243
    • 12470244
    • 12470257
    • 12470258
    • 12470259
    • 12470262
    • 12470268
    • 12470273
    • 12470279
    • 12470281
    • 12470283
    • 12470285
    • 12470290
    • 12470294
    • 12470299
    • 12470301
    • 12470303
    • 12470304
    • 12470305
    • 12470319
    • 12470320
    • 12470321
Amount recalled
36,881 infusion pumps

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

The connection between the beeper subassembly and the pump may fail. The GemStar infusion pump will identify this failure during the "self-test" while powering up which will result in a Beeper Error ("code 10/001/000"). This Beeper Error (code 10/001/000) is a service alarm that places the pump in an inoperable mode and requires service before it can be returned to service.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 30, 2016 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.