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Recall Observatory FDA recall evidence

Device product

Sterile Empty Vial and Injector (30mL PCA vial), Rx only, One/List No. 6021-03, Hospira, Inc., Lake Forest, IL 60045. For use with a compatible Hospira PCA pump set with injector and a compatible Hospira infusion device.

Z-2346-2012

August 02, 2012

Class II

Product summary

Firm
Hospira, Inc.
Event
Event 62909
Status
Terminated
Classification
Class II
Quantity
unknown
Official record key
device-enforcement:Z-2346-2012

Official wording

Reason: Reports of leaking during filling and administration.

Code information: The letter was issued for all product presently in the field and product that will be released. Specific lot numbers were not indicated in the letter.

Distribution pattern: Worldwide Distribution - USA including AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NY, NC, NK, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WY and the countries of Canada, Costa Rica and the Virgin Islands.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports of leaking during filling and administration.