Recall: D-598-2013

Class III - Minor Violations

Class IIIClassification

2013-04-26Initiated

TerminatedStatus

Teva Pharmaceuticals USA, Inc.Firm

Product

Amoxicillin for Oral Suspension, USP 400mg/5mL, NDC 0093-4161-78 (75ml) and 0093-4161-73 (100mL)

Reason

Discoloration: This recall is being carried out due to a yellow to brown discolored Amoxicillin powder on the inner foil seal of the bottles.

Distribution

Nationwide

Source: FDA drug enforcement report via openFDA (Voluntary: Firm initiated). If you take this product, talk to your pharmacist or doctor before stopping it.