DOBUTamine Injection
Discoloration; discolored solution from cracked vials
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Lack of sterility assurance
Cause type: Sterility / contamination
A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.
DOBUTAMINE, (a) 1080MG IN D5W 270ML, (b) 760MG IN D5W 190ML, ionotrop, used with a home pump, Rx only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
Drug: Dobutamine
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Discoloration; discolored solution from cracked vials
Discoloration: Firm received complaints of product discoloration and particulates.
Lack of Sterility Assurance.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of sterility assurance.
Lack of sterility assurance
Lack of sterility assurance
Lack of sterility assurance
Lack of sterility assurance
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