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
- Recalling Firm
- Teva Pharmaceuticals USA, Inc.
- 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.
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