FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Lupron Depot 22.5 mg 3 month Kit NDC 00074-3346-03 84 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
Kroger Specialty Pharmacy, Inc.
No ongoing recalls currently shown
Based on the official records currently available to Public Health Trace, no recalls naming Kroger Specialty Pharmacy, Inc. are currently shown as ongoing. The 67 records below are historical recall records.
Public Health Trace has 67 recalls naming Kroger Specialty Pharmacy, Inc. as the recalling firm, republished from official FDA and USDA sources.
Recall history - 67 terminated records
A bar chart of the number of recalls naming this company by year.
| Year | Recalls |
|---|---|
| 2018 | 67 |
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Kisqali 600 Dose 63 tablet 200 mg NDC 00078-0874-63 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
OPDIVO 40 mg/4 mL SDV NDC 00003-3772-11 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Tasigna Capsules 150 mg NDC 00078-0592-87 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Zarxio 300 mcg/0.5 mL PFS NDC 14 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Perjeta 420 mg/14 mL SDV Vials 50242-0145-01 21 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Letrozole 2.5 mg tab NDC 51991-0759-33 30 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Ondansetron 8 mg tablet NDC 57237-0076-30 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Bendeka 25 mg/mL 4 mL MDVPF NDC 63459-0348-04 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Capecitabine 500 mg Tablet NDC 00378-2512-78 28 days supply and 21 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Capecitabine 150 mg Tablet NDC 00378-2511-91 28 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass II
Imatinib Mesylate Tablet 400 mg NDC 60505-2901-03 30 days supply
- Reason
- Lack of Processing Controls.
- Published
- May 16, 2018
- Distribution
- Multiple states
Some FDA recall records on this page come from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
This page lists recalls that name Kroger Specialty Pharmacy, Inc. as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.
