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Recall Observatory FDA recall evidence

Drug product

R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 mL in 60 mL Syringe, Compounded by QuVa 519 Bloombury, NJ 08804, NDC 70092143350

D-1335-2020

April 23, 2020

Class III

Product summary

Firm
QuVa Pharma, Inc.
Event
Event 85547
Status
Terminated
Classification
Class III
Quantity
17,050 syringes
Official record key
drug-enforcement:D-1335-2020

Official wording

Reason: Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac

Code information: Lots: 30008721, Exp. 4/26/2020; 30008198, 30008554, Exp. 4/29/2020; 30008861, Exp. 4/30/2020; 30008859, Exp. 5/5/2020; 30008949, Exp. 5/10/2020; 30009073, Exp. 5/14/2020; 30009074, Exp. 30009138, Exp. 5/17/2020; 30009139, 30009227, Exp. 5/19/2020; 30009228, Exp. 5/20/2020; 30009387, 30009388, Exp. 5/27/2020; 30009410, 30009411, Exp. 5/28/2020; 30009413, Exp. 5/31/2020; 30009412, 30009489, Exp. 6/1/2020; 30009539, 30009563, Exp. 6/3/2020

Distribution pattern: Distributed Nationwide in the US.

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    Particulate Matter