Apothecary Products recalls medicine droppers with product code K508 due to potential glass particles on the dropper bulb. This could cause injury if the dropper is used. Affected units include those sold with lot number 021623 and UPC 07760:02005085.
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
Apothecary Products is recalling medicine droppers with product code K508 because glass particles might be on the outside of the dropper bulb. This could cause injury if the dropper is used. The recall affects units sold with lot number 021623 and UPC 077602005085.
Glass particles on the dropper bulb could cause injury if the dropper is used. The hazard is not described as causing serious injury in normal use, so it's a low-risk concern.
Parents and caregivers who use medicine droppers for children are most at risk. The recall applies to specific units sold with lot number 021623 and UPC 077602005085.
Check for product code K508 on the dropper. Affected units have lot number 021623 and UPC 077602005085.
Look for product code K508, lot number 021623, and UPC 077602005085 on the dropper.
The recall states there is a potential for glass particles on the dropper bulb, which could cause injury if used. However, the hazard is described as low risk.
Check for product code K508, lot number 021623, and UPC 077602005085 on the dropper.
The recall does not specify a remedy, so you can check if your dropper is affected and decide based on the product details.
We’ve drafted a message you can send Apothecary Products to request your refund or repair — edit it as you like.
Subject: Recall Z-1703-2023 — Apothecary Products Apothecary Products Hello, I own a Apothecary Products that is covered by recall Z-1703-2023 from Apothecary Products. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
