Kroger Specialty Pharmacy, Inc.
67 recalls on record · Latest: May 16, 2018
Kroger Specialty Pharmacy, Inc. Recall Insight
Kroger Specialty Pharmacy, Inc. appears on 67 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.080% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 16, 2018, which is the anchor point for assessing whether enforcement is currently active or historical.
On this page of 17 entries, severity tagging shows 0 critical, 17 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 17 of 17 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 2 distinct product categories, with issuing agencies dominated by FDA Drug (17). The date window on this page runs from May 16, 2018 to May 16, 2018.
Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.
Avonex 30 mcg/0.5 mL PFS Kit NDC 59627-0222-05 28 days supply
Kisqali 600 Dose 63 tablet 200 mg NDC 00078-0874-63 28 days supply
Prolia 60 mg/1 mL PF syringe NDC 55513-0710-01 180 days supply.
Cosentyx 150 mg/mL PFS 300 mg Dose NDC 00078-0639-98, 28 days supply
Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30
Dupixent 300 mg/2 mL PFS #2 w/ NS NDC 00024-5914-01 28 days supply
Creon DR 24,000 Units Capsule #250 NDC 00032-1224-07 30 days supply
Revlimid 25 mg oral cap NDC 59572-0425-21 28 days supply
Enbrel PFS 50 mg/mL Inj #4 NDC 58406-0435-04 28 days supply;
Praluent 75 mg Pen (2 pens/Pkg) NDC 00024-5901-02 28 days supply
Revlimid 5 mg oral cap NDC 59572-0405-28 28 days supply
Capecitabine 150 mg Tablet NDC 00378-2511-91 28 days supply
Letrozole 2.5 mg tab NDC 51991-0759-33 30 days supply
Xalkori 250 mg cap NDC 00069-8140-20 30 days supply
Tecfidera 240 mg capsule NDC 64406-0006-02 30 days supply
Temozolomide 20 mg NDC 43975-0253-05 28 days supply
Pediasure Liq. Vanilla G+G (CAN) #24 24 days supply, NDC 70074-0558-98
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