Reported Sep 13, 2017 · Terminated

Presource(R) Kits (custom surgical/procedural kits): The standard and custom kits are packed with all of the specific…

Cardinal Health 200, LLC

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: Cardinal Health 200, LLC · 1500 S Waukegan Rd · Waukegan, IL · 60085-6728

Is this the product you have?

  • Presource(R)
  • Kits (custom surgical/procedural kits)The standard and custom kits are packed with all of the specific disposable class I, II, and II implantable, life-supporting, or life-sustaining devices required by customers for common surgical and other medical procedures
Lot codes and dates

21 of 21 products

Products covered by this recall
Model / numberProduct as published
32CKIDK583449
5ABKKSL592789
5ABKKSL607318
5ACRKSM582954
5ACRKSM601437
5ACRKSM628559
5ANJKSJ583267
PNMHCFMCW 586498
PNMHCFMCW 632063
PNMHLMESS 581252
PNMHLMESS 616141
PNMHLMESS 651670
PNMHVPBHR 600959
PNMHVPBHR 621771
PNVZCRMFI 487007
PNVZCRMFJ 594611
PNVZCRMFJ 633632
PNVZLMMFL 498489
PNVZLMMFL 588152
PNVZLMMFM 610403
Amount recalled
184,102 kits

Where it was sold

  • Nationwide

Why it was recalled

The firm manufactured and distributed Presource(R) kits which contained BD SafetyGlide" 22GA 1¿ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection.

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 Jun 18, 2019 · Data as of Sep 19, 4:44 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.