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All product recalls associated with Hospira Inc..
Total Recalls
11
Past Year
0
Class I (Serious)
4
Most Recent
Apr 2017
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Presence of Particulate Matter: human hair found within an internal sample syringe.
Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.
Failed pH Specifications: Confirmed high out of specification (OOS) results for pH.
Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot number and/or expiration date to be faded or missing from the primary label on the glass vial.
Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report of an incorrect expiration date printed on the primary container labeled "01AUG1017" rather than "01AUG2017".
Failed Impurities/Degradation Specifications: Out of Specification(OOS) results for degradation product of etomidate was confirmed during stability testing.
Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.
Crystallization; identified as calcium salt of Ketorolac
Crystallization; identified as calcium salt of Ketorolac