Reported Feb 11, 2015 · Terminated

Plum A+ Infusion System with Hospira MedNet List 20792-04-25, Pole Clamp Assembly Part Number 820-95443-008. A cassette…

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?

  • Plum A+ Infusion System with Hospira MedNet List 20792-04-25, Pole Clamp Assembly Part Number 820-95443-008. A cassette based multi-function infusion system. Each system includes a pumping module and an assortment of disposable IV sets, optional accessories, and an operator's manual. The pole clamp assembly is used to provide a mechanism to tighten and loosen the grip of the pole clamp to remove the infuser from the IV pole.
Lot codes and dates
  • List Number20792-04-25
  • Serial Numbers

    102 of 102 codes

    • 17737372
    • 17737375
    • 17737377
    • 17737378
    • 17737383
    • 17737385
    • 17737390
    • 17737394
    • 17737395
    • 17737396
    • 17737397
    • 17737398
    • 17737399
    • 17737400
    • 17737402
    • 17737405
    • 17737408
    • 17737409
    • 17737414
    • 17737416
    • 17737419
    • 17737420
    • 17737421
    • 17737422
    • 17737424
    • 17737425
    • 17737426
    • 17737429
    • 17737430
    • 17737431
    • 17737432
    • 17737433
    • 17737435
    • 17737438
    • 17737440
    • 17737442
    • 17737443
    • 17737444
    • 17737445
    • 17737446
    • 17737447
    • 17737448
    • 17737449
    • 17737450
    • 17737451
    • 17737452
    • 17737454
    • 17737456
    • 17737458
    • 17737459
    • 17737460
    • 17737462
    • 17737463
    • 17737464
    • 17737467
    • 17737470
    • 17737475
    • 17737476
    • 17737478
    • 17737479
Amount recalled
102 infusors

This recall covers 2 products

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

Where it was sold

Why it was recalled

Plum A+ infusion system pole clamp assemblies were discovered to be cracked. If the knob on the pole clamp assembly is cracked, the infuser cannot be attached to the IV pole since the knob is used to tighten and loosen the grip of the pole clamp to the pole.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 28, 2016 · Data as of Sep 19, 5:28 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.