The Recall Desk
ModerateFDA (Drugs)·D-0456-2026·Announced 2026-04-22

Exchange Select honey lemon cough drops recalled after facility inspection findings

Exchange Select Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

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: 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

Exchange Select Menthol Cough Suppressant Oral Anesthetic Cough Drops in honey lemon flavour, 30-count bags, are being recalled. The product was manufactured for the military exchanges by Medical Group Care, LLC of Naples, Florida, and made in China. The NDC is 83698-580-30 and the UPC is 614299398870.

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 20241030, expiry 10/30/2026. 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
HONEY LEMON FLAVOR COUGH DROP (HONEY LEMON FLAVOR COUGH DROP)
Brand
HONEY LEMON FLAVOR COUGH DROP

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 # 20241030
  • Exp Date: 10/30/2026

UPCs (1)

  • 614299398870

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 →