Cefdinir for Oral Suspension, 125 mg/5 mL, packaged in a) 60 mL bottle (NDC 0093-4136-64); b) 100 mL bottle (NDC 0093-4136-73), Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960.
Reported: April 17, 2013 Initiated: February 26, 2013 #D-247-2013
Product Description
Cefdinir for Oral Suspension, 125 mg/5 mL, packaged in a) 60 mL bottle (NDC 0093-4136-64); b) 100 mL bottle (NDC 0093-4136-73), Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960.
Reason for Recall
Defective Container: This recall is being carried out due to the potential for improperly sealed bottles.
Details
- Recalling Firm
- Teva Pharmaceuticals USA, Inc.
- Units Affected
- 62,187 bottles
- Distribution
- Nationwide
- Location
- Sellersville, PA
Frequently Asked Questions
What product was recalled? ▼
Cefdinir for Oral Suspension, 125 mg/5 mL, packaged in a) 60 mL bottle (NDC 0093-4136-64); b) 100 mL bottle (NDC 0093-4136-73), Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960.. Recalled by Teva Pharmaceuticals USA, Inc.. Units affected: 62,187 bottles.
Why was this product recalled? ▼
Defective Container: This recall is being carried out due to the potential for improperly sealed bottles.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 17, 2013. Severity: Moderate. Recall number: D-247-2013.
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