The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-1714-2019·Announced 2019-08-14

RXQ Compounding Recalls TURBO DROPS Ophthalmic Solution Due to Sterility Concerns

RXQ Compounding LLC is recalling TURBO DROPS ophthalmic solution because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class II. According to the rubric, FDA Class II recalls involving significant injury/property-damage reports or hospitalization are rated Severe (4). While no injuries are explicitly reported in the text, the lack of sterility assurance in an ophthalmic product poses a significant risk of serious harm (infection), aligning with the Severe criteria for high-risk drug recalls.

Plain-English summary

RXQ Compounding LLC is recalling TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN, 5 ML per dropper bottle. The recall is being conducted because the product lacks assurance of sterility. The affected product is identified by NDC 70731-0206-05.

The recall includes all lots within expiry. The product was distributed nationwide in the United States. The source text does not specify the number of units recalled or the specific dates of distribution.

Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions. The source text does not report any illnesses or injuries associated with the use of this product.

The recalled product

Product
TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN, 5 ML per dropper bottle, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC 70731-0206-05
Manufacturer
RXQ Compounding LLC
Category
Drug — Ophthalmic Solution
Hazard

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 →

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