QuVa Pharma recalls R.E.C.K. (Ropivacaine HCl, Epinephrine, Clonidine HCl, Ketorolac Tromethamine) in Sodium Chloride Solution for periarticular use due to particulate matter. This compounded drug may cause blockages if injected.
Presence of Particulate Matter
QuVa Pharma is recalling a specific compounded medication called R.E.C.K. for periarticular use. The product contains particulate matter, which could cause blockages if injected into the body.
Particulate matter in the medication can cause blockages when injected into the body. This may lead to complications such as tissue damage or reduced effectiveness of the medication.
People who have the recalled R.E.C.K. injection (50 mL syringe) for periarticular use. Patients receiving this medication for pain relief are most at risk.
Check for the product name 'R.E.C.K.' (Ropivacaine HCl, Epinephrine, Clonidine HCl, and Ketorolac Tromethamine) in 50 mL syringes. The NDC code is listed as 70092-1433-50 with specific lot numbers and expiration dates provided in the recall notice.
Verify the NDC code (70092-1433-50) and lot numbers listed in the recall notice to confirm if your medication is affected.
The recall indicates the presence of particulate matter, which could cause blockages if injected. Do not use the product until you confirm it's not recalled.
Check the NDC code and lot numbers listed in the recall notice to determine if your product is affected. If it is, stop using it and contact QuVa Pharma for further instructions.
Look for the NDC code 70092-1433-50 with the specific lot numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send QuVa Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0113-2026 — QuVa Pharma QuVa Pharma Hello, I own a QuVa Pharma that is covered by recall D-0113-2026 from QuVa Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
