Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ROPivacaine HCl 0.2% PF in Sodium Chloride 1 Recalled by STAQ Pharma, Inc. Due to STAQ Pharma Inc. received consumer complaints related to...
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 STAQ Pharma, Inc. directly.
Affected Products
ROPivacaine HCl 0.2% PF in Sodium Chloride 1,000 mg/500 mL (2 mg per mL) Injection, 500 mL bags, Rx only, STAQ Pharma Inc. 14135 E 42nd Ave, Unit 50, Denver, Colorado 80239, NDC 73177-0109-26,
Quantity: 2616 bags
Why Was This Recalled?
STAQ Pharma Inc. received consumer complaints related to leaking bags and other potential bag concerns. Upon investigation, they determine the source of the issue was with the bag manufacturer who released bags Lot # 134142-001A which had failed internal QC tests for leaks.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About STAQ Pharma, Inc.
STAQ Pharma, Inc. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report