Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories
Reported: July 17, 2019 Initiated: May 9, 2019 #D-1467-2019
Product Description
Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories
Reason for Recall
GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Details
- Recalling Firm
- American Health Packaging
- Units Affected
- 375,921 bottles
- Distribution
- Nationwide USA
- Location
- Columbus, OH
Frequently Asked Questions
What product was recalled? ▼
Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories. Recalled by American Health Packaging. Units affected: 375,921 bottles.
Why was this product recalled? ▼
GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 17, 2019. Severity: Moderate. Recall number: D-1467-2019.
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