The presence of brown liquid was found in some vials instead of white or almost white powder, indicating a serious quality defect that may affect the product’s safety and efficacy. Potential effects: lack of treatment efficacy, infections, severe complications after intravenous administration.
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Important Information
Do not use the product from batch 0710624, check the batch number on the packaging, return packs from this batch to the pharmacy, and if the medicine from the defective batch has been used and any ala...
Withdrawal from the market throughout the country of batch 0710624 of Cefazolin TZF, prohibition of placing this batch on the market, and granting the decision immediate enforceability.
If you feel unwell after consuming this product, contact your doctor or call the poison control center.
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