Orkambi 200 mg/125 mg Tablets #112 NDC 51167-0809-01 28 days supply.
Reported: May 16, 2018 Initiated: April 3, 2018 #D-0750-2018
Product Description
Orkambi 200 mg/125 mg Tablets #112 NDC 51167-0809-01 28 days supply.
Reason for Recall
Lack of Processing Controls.
Details
- Recalling Firm
- Kroger Specialty Pharmacy, Inc.
- Units Affected
- Unknown
- Distribution
- MS, LA, AR, IL, FL
- Location
- Vicksburg, MS
Frequently Asked Questions
What product was recalled? ▼
Orkambi 200 mg/125 mg Tablets #112 NDC 51167-0809-01 28 days supply.. Recalled by Kroger Specialty Pharmacy, Inc.. Units affected: Unknown.
Why was this product recalled? ▼
Lack of Processing Controls.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 16, 2018. Severity: Moderate. Recall number: D-0750-2018.
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