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
Reported: July 1, 2020 Initiated: April 23, 2020 #D-1335-2020
Product Description
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
Reason for Recall
Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Details
- Recalling Firm
- QuVa Pharma, Inc.
- Units Affected
- 17,050 syringes
- Distribution
- Distributed Nationwide in the US.
- Location
- Sugar Land, TX
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by QuVa Pharma, Inc.. Units affected: 17,050 syringes.
Why was this product recalled? ▼
Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 1, 2020. Severity: Low. Recall number: D-1335-2020.
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