QC Quality Choice Saline Nasal Gel Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling QC Quality Choice Saline Nasal Gel with Soothing Aloe due to manufacturing deviations that could impact product quality.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Product Quest Manufacturing LLC is voluntarily recalling 4,200 tubes of QC Quality Choice, Saline Nasal Gel with Soothing Aloe, 0.5 OZ (14.1 g). The product is distributed by C.D.M.A., Inc., and was sold nationwide in the USA. The recall covers all lots remaining within their expiry dates.
The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations. These deviations indicate that the products were manufactured under conditions that could impact product quality. The source text does not report any specific illnesses or injuries associated with this recall.
Consumers who have purchased this product should stop using it and contact the distributor or retailer for a refund or replacement. The product can be identified by the UPC 6 35515 99202 3.
The recalled product
- Product
- QC Quality Choice, Saline Nasal Gel with Soothing Aloe, 0.5 OZ (14.1 g) tube, Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376-0995, UPC 6 35515 99202 3.
- Manufacturer
- Product Quest Manufacturing LLC
- Category
- Drug — Nasal Gel
- Hazard
- Affected units
- 4,200
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 remaining within expiry.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 54 recalled by Product Quest Manufacturing 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.
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