Carie Boyd's Prescription Shop recalls LET Gel (Lidocaine/Epinephrine/Tetracaine Topical Gel) due to incorrect formulation. This product may contain unsafe levels of active ingredients. Consumers should contact the manufacturer for details.
Product Mix-up: Incorrect Product Formulation
Carie Boyd's Prescription Shop has recalled LET Gel topical gel because it was mixed up with the wrong formulation. This could lead to unsafe levels of medication being applied to the skin.
The gel was manufactured with incorrect ingredient concentrations. This could result in skin irritation or adverse reactions if used as intended. The risk is not severe enough to cause serious injury in normal use.
People who purchased this specific LET Gel product from Carie Boyd's Prescription Shop. Those with sensitive skin or using the product for medical purposes are at slightly higher risk.
Check for the product name 'LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel)' on the label. Look for the lot number 09202023@7 and expiration date 03/18/2024.
Look for the product name and lot number 09202023@7 on the label to confirm if it's recalled.
The product has been recalled due to an incorrect formulation, but it may still be safe for some users. Contact the manufacturer for specific guidance.
The recall record does not specify a remedy, so contact Carie Boyd's Prescription Shop directly for instructions.
Check the label for the product name 'LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel)' and lot number 09202023@7.
We’ve drafted a message you can send Carie Boyd's Prescription Shop to request your refund or repair — edit it as you like.
Subject: Recall D-0140-2024 — Carie Boyd's Prescription Shop Carie Boyd's Prescription Shop Hello, I own a Carie Boyd's Prescription Shop that is covered by recall D-0140-2024 from Carie Boyd's Prescription Shop. 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.
