STAQ Pharma recalls 500mL ROPivacaine HCl 0.2% injection bags with leaking issues. These bags were manufactured by a third party and failed quality checks. Consumers should check lot numbers on the packaging.
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.
STAQ Pharma is recalling 500mL ROPivacaine HCl 0.2% injection bags that may leak. The leak risk comes from bags produced by a third-party manufacturer that failed internal quality tests. This could lead to contamination or improper medication delivery if the bag leaks during use.
The bags were manufactured by a third party that failed internal quality tests for leaks. Leaking bags could cause medication contamination or improper delivery during medical procedures if the bag leaks while being used.
Prescription drug users who have the specific 500mL ROPivacaine HCl 0.2% injection bags with lot numbers 23109472A through 23109522A. Healthcare providers and patients using these bags for medical procedures are most at risk.
Check the lot number on the bag, which is listed as 23109472A through 23109522A. The product is a 500mL injection bag labeled for prescription use only, with specific expiration dates.
Look for the lot number on the bag, which should be one of 23109472A through 23109522A.
STAQ Pharma received consumer complaints about leaking bags and determined the issue was due to a third-party manufacturer that failed internal quality tests for leaks.
Check the lot number on the bag. If it matches the listed lot numbers, contact STAQ Pharma for further instructions.
The recall is for potential leaks, which could lead to medication contamination or improper delivery during medical procedures, but the hazard level is low risk as the bags are not expected to leak under normal use conditions.
We’ve drafted a message you can send STAQ Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0147-2024 — STAQ Pharma STAQ Pharma Hello, I own a STAQ Pharma that is covered by recall D-0147-2024 from STAQ 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.
