PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: June 19, 2013 Initiated: April 26, 2013 #D-598-2013

Product Description

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

Reason for Recall

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

Details

Units Affected
758,554 bottles
Distribution
Nationwide
Location
Sellersville, PA

Frequently Asked Questions

What product was recalled?
Amoxicillin for Oral Suspension, USP 400mg/5mL, NDC 0093-4161-78 (75ml) and 0093-4161-73 (100mL). Recalled by Teva Pharmaceuticals USA, Inc.. Units affected: 758,554 bottles.
Why was this product recalled?
Discoloration: This recall is being carried out due to a yellow to brown discolored Amoxicillin powder on the inner foil seal of the bottles.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 19, 2013. Severity: Low. Recall number: D-598-2013.