CLASS III Drug recall · Reported 13 Dec 2023 · FDA Enforcement Report
LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine recalled
Right Value Drug Stores is recalling LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), distributed nationwide in the US. The recall was initiated on 9 Nov 2023 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0140-2024
- FDA event ID
- 93316
- Recalling firm
- Right Value Drug Stores, Irving, TX
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 9 Nov 2023
- FDA classified
- 6 Dec 2023
- Reported
- 13 Dec 2023
- Type
- Voluntary: Firm initiated
- Reason category
- Packaging Defects
- Drug class
- Pain Medication
Timeline
| 9 Nov 2023 | Recall initiated by company | |
| 6 Dec 2023 | Classified by FDA | +27 days |
| 13 Dec 2023 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product Mix-up: Incorrect Product Formulation
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), Single-use Topical Syringe, 3mL syringe, 10/pack, Rx only, Carie Boyd Pharmaceuticals, 8400 Esters Blvd, Ste# 190, Irving, TX 75063, NDC73271-1003-1
Where it was distributed
USA Nationwide
Questions about this recall
Why was it recalled?
Product Mix-up: Incorrect Product Formulation
Which lots are affected?
Lot#: 09202023@7, Exp 03/18/2024
Where was it sold?
USA Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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