glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10
Reported: March 8, 2017 Initiated: January 19, 2017 #D-0491-2017
Product Description
glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10
Reason for Recall
Presence of Foreign Tablets/Capsules; bottles of Glipizide 5 mg tablets may contain Glipizide 10 mg tablets
Details
- Recalling Firm
- Mylan Pharmaceuticals Inc.
- Units Affected
- 1338 bottles
- Distribution
- Nationwide
- Location
- Morgantown, WV
Frequently Asked Questions
What product was recalled? ▼
glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10. Recalled by Mylan Pharmaceuticals Inc.. Units affected: 1338 bottles.
Why was this product recalled? ▼
Presence of Foreign Tablets/Capsules; bottles of Glipizide 5 mg tablets may contain Glipizide 10 mg tablets
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 8, 2017. Severity: Moderate. Recall number: D-0491-2017.
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