Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported December 13, 2023
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
Product Mix-up: Incorrect Product Formulation
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop recalled LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), … - a low-severity action.
LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), … was recalled by Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop in December 13, 2023. Reason: Product Mix-up: Incorrect Product Formulation. Check the official notice for the remedy. Verify recall #D-0140-2024 with the FDA Drug before acting.
The recall
Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop issued this low-severity FDA Drug recall-Product Mix-up: Incorrect Product Formulation.
- Low
- severity level
- Class III
- classification
- December 13, 2023
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0140-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0140-2024) was formally reported on December 13, 2023, with the manufacturer initiating the action on November 9, 2023. It is classified under Low severity (Class III), with a current status of Terminated. Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop is listed as the recalling firm, operating out of Irving, TX. Federal records list the affected scope as 190 syringes.
The documented reason for this recall is: Product Mix-up: Incorrect Product Formulation Distribution data in the federal record shows the product reached: USA Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
190 syringes
Related Recalls
6
0 from same agency
Product description
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
Reason for recall
Product Mix-up: Incorrect Product Formulation
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0140-2024 |
| Date reported | December 13, 2023 |
| Date initiated | November 9, 2023 |
| Recalling firm | Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop |
| Firm location | Irving, TX |
| Affected scope | 190 syringes |
| Distribution | USA Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0140-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop. Units affected: 190 syringes.
Why was this product recalled? ▼
Product Mix-up: Incorrect Product Formulation
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 13, 2023. Severity: Low. Recall number: D-0140-2024.
Where was the recalled product distributed? ▼
Distribution: USA Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0140-2024) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported December 13, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.