Startseite/Alle Rückrufe/FDA-D-0465-2026
FDA DrugsClass II

QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, Distributed By: CDMA, Inc., Novi MI 48375, Made in China, NDC: 83698-616-25, UPC: 635515993372.

Veröffentlicht: 22. April 2026Rückruf-ID: D-0465-2026Kategorie: Arzneimittel & MedikamenteLand: Vereinigte Staaten
US
PharmaceuticalFDA DrugsUSUS

QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, Distributed By: CDMA, Inc., Novi MI 48375, Made in China, NDC: 83698-616-25, UPC: 635515993372.

Recalling Firm: Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.

Produktbeschreibung & Identifikation

QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, Distributed By: CDMA, Inc., Novi MI 48375, Made in China, NDC: 83698-616-25, UPC: 635515993372.

Additional Source Details

FieldValue
CityXiamen
StateN/A
Openfda › Upc › 10635515993372
Openfda › Upc › 2635515993372
Openfda › UniiL7T10EIP3A
Openfda › RouteORAL
Openfda › Rxcui359751
Openfda › Spl id47189e74-0106-9a03-e063-6394a90addf4
Openfda › Brand nameQUALITY CHOICE
Openfda › Spl set id2307f3a7-f6e7-8a5d-e063-6394a90ab7eb
Openfda › Package ndc › 183698-616-25
Openfda › Package ndc › 26355159933
Openfda › Product ndc83698-616
Openfda › Generic nameCOUGH DROPS HONEY LEMON SUGAR FREE
Openfda › Product typeHUMAN OTC DRUG
Openfda › Substance nameMENTHOL
Openfda › Manufacturer nameXiamen Kang Zhongyuan Biotechnology Co., Ltd.
Openfda › Application numberM012
Openfda › Is original packagertrue
Event id98648
Address 1No. 2018
Address 22 Jietou Road
Code infoLot # 20240524, Exp Date: 05/24/2026; Lot # 20240720, Exp Date: 07/20/2026.
Postal codeN/A
Report date20260422
Product typeDrugs
Product quantityN/A
Reason for recallThis recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260320
Initial firm notificationLetter
Center classification date20260410

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, Distributed...?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Übersicht

  • Rückrufendes UnternehmenXiamen Kang Zhongyuan Biotechnology Co., Ltd.
  • StatusOngoing
  • RisikostufeClass II
  • DistributionUS Nationwide.
Recall Hazard Severity
High Alert (Class I)
Offizielle Behördenwarnung

📢 Warnung teilen

Alert family and friends to keep them safe. Copy this quick alert message:

🚨 SAFETY ALERT: Xiamen Kang Zhongyuan Biotechnology Co., Ltd. - QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, Distributed By: CDMA, Inc., Novi MI 48375, Made in China, NDC: 83698-616-25, UPC: 635515993372.

Check if your household is affected:
https://therecallfile.com/de/recalls/qc-quality-choice-menthol-cough-suppressant-oral-anesthetic-cough-drop/FDA-D-0465-2026
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