Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
R.E.C.K. (Ropivacaine Recalled by QuVa Pharma, Inc. Due to Presence of Particulate Matter: Fresenius Kabi recalling vials...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact QuVa Pharma, Inc. directly.
Affected Products
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
Quantity: 17,050 syringes
Why Was This Recalled?
Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About QuVa Pharma, Inc.
QuVa Pharma, Inc. has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report