Quality Choice strawberry throat drops recalled after facility inspection findings
QC Quality Choice Pectin Oral Demulcent Throat Soothing Drops, creamy strawberry flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
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 2/5 (Moderate).
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: Precautionary recall prompted by facility inspection observations that may bear on product quality, with no specific product defect described, which fits the Moderate band.
Plain-English summary
QC Quality Choice Pectin Oral Demulcent Throat Soothing Drops in creamy strawberry flavour, 30-count bags, are being recalled. The product is distributed by CDMA, Inc. of Novi, Michigan and made in China. The NDC is 83698-625-30 and the UPC is 635515999398.
The recall is being initiated following FDA's recommendation, based on certain observations noted during an inspection of the manufacturing facility on 15 August 2025 that may bear on product quality. The FDA classified the action as Class II. The source does not describe any specific defect found in the product itself.
The affected lot is 20240720, expiry 07/20/2026. Distribution was US nationwide.
Consumers who have the affected lot should stop using it and contact the retailer where it was purchased.
The recalled product
- Product
- QUALITY CHOICE COUGH DROPS CREAMY STRAWBERRY (COUGH DROPS CREAMY STRAWBERRY)
- Brand
- QUALITY CHOICE COUGH DROPS CREAMY STRAWBERRY
- Manufacturer
- Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
- Category
- Drug — Throat drops
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 (2)
- Lot # 20240720
- Exp Date: 07/20/2026.
UPCs (1)
- 635515999398
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 15 recalled by Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 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 15 products in this recall →Related recalls
Same manufacturer · Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
See all →- ModerateMGC Health sugar free honey lemon cough drops recalled after inspection
FDA (Drugs) · 2026-04-22
- ModerateQuality Choice sugar free black cherry cough drops recalled after inspection findings
FDA (Drugs) · 2026-04-22
- ModerateMenthol Flavor Cough Drops Recalled Due to Potential Product Quality Issues
FDA (Drugs) · 2026-04-22
- ModerateQuality Choice menthol cough drops recalled after facility inspection findings
FDA (Drugs) · 2026-04-22
- ModerateMGC Health 80-count honey lemon cough drops recalled after inspection findings
FDA (Drugs) · 2026-04-22
Same hazard · facility inspection
See all →- ModerateQuality Choice cherry cough drops recalled after facility inspection findings
FDA (Drugs) · 2026-04-22
- ModerateMGC Health 30-count honey lemon cough drops recalled after inspection findings
FDA (Drugs) · 2026-04-22
- ModerateCaring Mill cherry cough drops recalled after facility inspection findings
FDA (Drugs) · 2026-04-22
Similar recalls
- ModerateQC Quality Choice Saline Nasal Gel Recalled for Quality Deviations
FDA (Drugs) · 2018-10-24
- HighQuality Choice moisturizing relief eye drops recalled over sterility assurance
FDA (Drugs) · 2026-04-08
- HighQuality Choice irritation relief eye drops recalled over sterility assurance
FDA (Drugs) · 2026-04-08
- SevereClinical Specialties Compounding Pharmacy Recalls Laser Ophthalmic Drops
FDA (Drugs) · 2013-07-10
- HighClinical Specialties Compounding Pharmacy Recalls Cataract Drops Due to Sterility Concerns
FDA (Drugs) · 2013-07-10
- ModerateProduct Quest Recalls QC Quality Choice Saline Nasal Spray for CGMP Deviations
FDA (Drugs) · 2018-10-24