The Recall Desk
SevereFDA (Drugs)·D-1711-2019·Announced 2019-08-14

RXQ Compounding Recalls Travasol 10% Injection Due to Sterility Concerns

RXQ Compounding LLC is recalling Travasol 10% Injection Solution because the product lacks assurance of sterility.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a lack of assurance of sterility in an injectable product, which poses a significant risk of serious injury or infection, meeting the criteria for a Severe rating.

Plain-English summary

RXQ Compounding LLC is recalling Travasol 10% (Amino Acid) Injection Solution, 50 ML per Vial. The recall was initiated because the product lacks assurance of sterility. The affected product is identified by NDC 70731-0151-50 and includes all lots within their expiry dates.

The recall is classified as Class II by the U.S. Food and Drug Administration. The distribution pattern is listed as Nationwide USA. No specific lot numbers or dates are provided in the source text beyond the general instruction to check all lots within expiry.

Healthcare providers and patients should stop using the recalled product and contact their pharmacist or healthcare provider for further instructions. Consumers should not attempt to use the product if they are unsure of its sterility status.

The recalled product

Product
TRAVASOL 10% (AMINO ACID) INJECTION SOLUTION, 50 ML per Vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 70731-0151-50

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All lots within expiry

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 86 recalled by RXQ Compounding LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 86 products in this recall →