Class III
Terminated
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
This recall has been terminated (originally issued July 1, 2020).
- Company
- Quva Pharma, Inc.
- Recall Initiated
- April 23, 2020
- Posted
- July 1, 2020
- Recall Number
- D-1335-2020
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 17,050 syringes
- Firm Location
- Sugar Land, TX, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Distribution
Distributed Nationwide in the US.
Lot / Code Info
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
More recalls by Quva Pharma, Inc.
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