Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Fagron, Inc: LETS GEL KIT Recalled for Microbial Contamination

Agency Publication Date: November 29, 2019
Share:
Sign in to monitor this recall

Summary

Fagron, Inc. is recalling 11,912 LETS GEL KIT Convenience Packs used to prepare 100 mL of LETS GEL for prescription compounding. These kits, which contain medications including Lidocaine, Epinephrine, and Tetracaine, have been found to have microbial contamination in a non-sterile product. Consumers who have these kits should not use them for compounding or medical procedures and should immediately contact their healthcare provider or pharmacist.

Risk

The presence of microbial contamination in these medication kits poses a risk of infection to patients. Because these kits are used for compounding topical gels typically applied to skin or open wounds, the introduction of bacteria or other microbes could lead to serious medical complications.

What You Should Do

  1. Check your LETS GEL KIT (To prepare 100 mL LETS GEL) for NDC: 51552-1539-1 and the following lot numbers: 18F25-U03-044296, 18F25-U04-044297, 18H22-U06-045284, 18I24-U05-045853, 18K06-U03-047041, 18K06-U04-047042, 18K27-U11-047460, 18K28-U10-047519, 19A06-U02-048182, 19A06-U03-048183, 19A16-U13-048363, 19A21-U02-048503, 19B10-U02-048787, 19B14-U05-048781, 19C05-U01-049199, 19C05-U02-049200, 19C11-U07-049451, 19C25-U02-048758, 19D07-U01-049884, 19D07-U02-049885, 19E09-U01-050298, 19E23-U01-050763, 19F16-U12-000052, 19F16-U13-000053, 19G07-U01-000357, 19G07-U02-000358, 19G21-U01-000930, 19G21-U02-000931, 19H01-U01-001172, 19H01-U02-001174, 19I03-U01-002019, 19I03-U02-002020, or 19I03-U03-002021.
  2. Verify the expiration dates printed on your package which range from 11/8/2019 to 2/4/2021.
  3. Stop using the affected product immediately and do not use it for prescription compounding or patient treatment.
  4. Contact your healthcare provider or pharmacist for guidance regarding the use of this product and return any unused kits to the place of purchase for a refund.
  5. Contact Fagron, Inc. at their Saint Paul facility (651-636-5050) or visit www.fagron.com for further instructions regarding the return process.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Drug product return and reimbursement

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL)
Model:
NDC: 51552-1539-1
Recall #: D-0533-2020
Lot Numbers:
18F25-U03-044296 (Exp 11/8/2019)
18F25-U04-044297 (Exp 11/8/2019)
18H22-U06-045284 (Exp 1/24/2020)
18I24-U05-045853 (Exp 11/8/2019)
18K06-U03-047041 (Exp 1/24/2020)
18K06-U04-047042 (Exp 1/24/2020)
18K27-U11-047460 (Exp 3/16/2020)
18K28-U10-047519 (Exp 3/16/2020)
19A06-U02-048182 (Exp 3/16/2020)
19A06-U03-048183 (Exp 3/16/2020)
19A16-U13-048363 (Exp 3/16/2020)
19A21-U02-048503 (Exp 3/16/2020)
19B10-U02-048787 (Exp 3/16/2020)
19B14-U05-048781 (Exp 3/16/2020)
19C05-U01-049199 (Exp 3/16/2020)
19C05-U02-049200 (Exp 3/16/2020)
19C11-U07-049451 (Exp 3/16/2020)
19C25-U02-048758 (Exp 3/16/2020)
19D07-U01-049884 (Exp 3/16/2020)
19D07-U02-049885 (Exp 3/16/2020)
19E09-U01-050298 (Exp 3/16/2020)
19E23-U01-050763 (Exp 9/11/2020)
19F16-U12-000052 (Exp 9/11/2020)
19F16-U13-000053 (Exp 10/24/2020)
19G07-U01-000357 (Exp 10/24/2020)
19G07-U02-000358 (Exp 10/24/2020)
19G21-U01-000930 (Exp 10/24/2020)
19G21-U02-000931 (Exp 12/17/2020)
19H01-U01-001172 (Exp 12/17/2020)
19H01-U02-001174 (Exp 12/17/2020)
19I03-U01-002019 (Exp 2/4/2021)
19I03-U02-002020 (Exp 2/4/2021)
19I03-U03-002021 (Exp 12/17/2020)
Date Ranges: November 8, 2019 - February 4, 2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84179
Status: Resolved
Manufacturer: Fagron, Inc
Sold By: Fagron, Inc.; Prescription compounding pharmacies
Manufactured In: United States
Units Affected: 11,912 kits
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.