Kramer Laboratories recalls Safe Tussin DM cough and chest congestion medicine due to potential non-food grade lubricant in mixing vessels. Affected lots from 2020 expire 10/2023 or 8/2: stop using immediately.
CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Kramer Laboratories is recalling Safe Tussin DM cough and chest congestion medicine because it may contain non-food grade lubricant during manufacturing. This could pose a risk to consumers if the product is ingested.
The product was made using non-food grade lubricant in the mixing vessel, which could contaminate the medicine. If ingested, this lubricant might cause health issues, particularly in children who are more vulnerable to such contaminants.
People who bought Safe Tussin DM cough and chest congestion medicine from Kramer Laboratories in 2020, especially those with the specific lot numbers listed. Children and infants are at higher risk due to potential ingestion of harmful substances.
Check the product label for the lot numbers 8753, 8753A, or 8659. The expiration dates are either 10/2023 or 8/2023. The product is packaged in 4.0 fl oz (118mL) containers.
Discard the product if you have the affected lot numbers listed in the recall notice.
No, the product may contain non-food grade lubricant that could be harmful if ingested, especially in children.
Lot numbers 8753, 8753A, and 8659 from Kramer Laboratories in 2020.
Check the product label for the lot numbers 8753, 8753A, or 8659 with expiration dates of 10/2023 or 8/2023.
We’ve drafted a message you can send Kramer Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0942-2023 — Kramer Laboratories Kramer Laboratories Hello, I own a Kramer Laboratories that is covered by recall D-0942-2023 from Kramer Laboratories. 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.
