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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

QuVa Pharma R.E.C.K. Syringes Recalled for Particulate Matter

Agency Publication Date: October 27, 2025
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Summary

QuVa Pharma, Inc. is recalling 75,885 syringes of R.E.C.K. (ropivacaine HCl, epinephrine, clonidine HCl, and ketorolac tromethamine) in Sodium Chloride Solution (50 mL syringes). The recall was initiated because particulate matter was found in the solution. This compounded medication is an injection intended for periarticular use (around a joint) and is not for intravenous use.

Risk

The presence of particulate matter in an injectable drug can cause local inflammation, tissue damage, or small vessel blockages if the particles are injected into the body. While no injuries have been reported, the contamination poses a medium risk to patient safety.

What You Should Do

  1. Stop using the recalled product immediately.
  2. Check the medication label for the product name 'R.E.C.K.' (Ropivacaine HCl, EPINEPHrine, CloNIDine HCl, and Ketorolac Tromethamine) in 50 mL syringes with NDC 70092-1433-50.
  3. Identify affected units by checking the lot number and expiration date printed on the syringe or outer packaging. See the Affected Products section below for the full list of affected codes.
  4. Contact the manufacturer, QuVa Pharma, Inc., or your distributor to arrange for the return of any unused syringes.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions or to report adverse events.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: R.E.C.K. (Ropivacaine HCl, EPINEPHrine, CloNIDine HCl, and Ketorolac Tromethamine) in Sodium Chloride Solution (50 mL syringe)
Variants: Compounded Drug, Injection
Lot Numbers (239):
10149179 (exp 10/15/2025)
10149503 (exp 10/13/2025)
10149504 (exp 10/13/2025)
10149657 (exp 10/16/2025)
10149658 (exp 10/16/2025)
10149659 (exp 10/15/2025)
10150137 (exp 10/23/2025)
10150138 (exp 10/23/2025)
10150139 (exp 10/23/2025)
10150140 (exp 10/23/2025)
10149729 (exp 10/16/2025)
10149730 (exp 10/16/2025)
10149732 (exp 10/16/2025)
10149733 (exp 10/16/2025)
10149737 (exp 10/16/2025)
10149738 (exp 10/16/2025)
10149790 (exp 10/17/2025)
10149787 (exp 10/16/2025)
10149788 (exp 10/16/2025)
10149791 (exp 10/17/2025)
10149792 (exp 10/16/2025)
10149800 (exp 10/16/2025)
10149841 (exp 10/19/2025)
10149833 (exp 10/19/2025)
10149840 (exp 10/19/2025)
10149842 (exp 10/20/2025)
10149838 (exp 10/19/2025)
10149839 (exp 10/19/2025)
10149843 (exp 10/20/2025)
10149968 (exp 10/20/2025)
10149969 (exp 10/21/2025)
10150007 (exp 10/22/2025)
10150134 (exp 10/23/2025)
10150253 (exp 10/26/2025)
10150254 (exp 10/26/2025)
10150135 (exp 10/23/2025)
10150302 (exp 10/27/2025)
10150303 (exp 10/28/2025)
10150182 (exp 10/31/2025)
10150183 (exp 10/23/2025)
10150185 (exp 10/24/2025)
10150184 (exp 10/23/2025)
10150186 (exp 10/23/2025)
10150187 (exp 10/23/2025)
10150204 (exp 10/27/2025)
10150357 (exp 10/29/2025)
10150358 (exp 10/29/2025)
10150361 (exp 10/29/2025)
10150362 (exp 10/29/2025)
10150525 (exp 10/30/2025)
NDC:
70092-1433-50

QuVA Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, TX 77478. THIS IS A COMPOUNDED DRUG.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97790
Status: Active
Manufacturer: QuVa Pharma, Inc.
Sold By: Hospitals; Surgical centers; Wholesalers
Manufactured In: United States
Units Affected: 75,885 syringes
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.