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
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Low RiskFDA Drug
Medications & Supplements/Over-the-Counter

Idelle Labs: SURE Antiperspirant & Deodorant Recalled for Incorrect Active Ingredient

Agency Publication Date: January 8, 2020
Share:
Sign in to monitor this recall

Summary

Idelle Labs is recalling various SURE 48hr Confidence invisible solid and original solid Antiperspirant & Deodorant products because the active ingredient listed on the label does not match the actual active ingredient contained in the product. This labeling error means consumers are using a different medication than they intended, though the quantities affected were not specified. If you own these products, you should stop using them and contact your healthcare provider or pharmacist for guidance.

Risk

The product contains an undeclared active pharmaceutical ingredient (API) that differs from what is stated on the packaging, which may lead to ineffective treatment or unexpected reactions if a consumer is sensitive to the actual ingredient used.

What You Should Do

  1. Check your product packaging for the following UPC codes and Lot numbers: SURE Unscented Invisible Solid (UPC 883484717172, Lots 19273K1, 19274K1, 19274K2, 19725K1, 19725K2, 19726K1), SURE Nourishing Coconut (UPC 883484310205, Lot 19277K1), SURE Regular Original Solid (UPC 883484717936, Lots 19279K1, 19279K2, 19280K1), or SURE Unscented Original Solid (UPC 883484717943, Lots 19277K2, 19278K1).
  2. Stop using the affected deodorant product immediately if it matches the identified lot numbers.
  3. Contact your healthcare provider or pharmacist for guidance regarding the use of this product and any potential skin reactions or concerns.
  4. Return any unused product to the pharmacy or place of purchase for a full refund.
  5. Contact the manufacturer, Idelle Labs, at their El Paso, Texas facility for further instructions.
  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

๐Ÿ’ฐFull Refund

Drug product refund and medical consultation

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

Affected Products

Product: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant (2.6 oz / 73g)
Model:
NDC# 41595-5509-2
UPC Codes:
883484717172
Lot Numbers:
19273K1
19274K1
19274K2
19725K1
19725K2
19726K1
Product: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & Deodorant (2.6 oz / 73g)
Model:
NDC# 41595-5547-1
UPC Codes:
883484310205
Lot Numbers:
19277K1
Product: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant (2.7 oz / 76g)
Model:
NDC# 41595-5514-1
UPC Codes:
883484717936
Lot Numbers:
19279K1
19279K2
19280K1
Product: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant (2.7 oz / 76g)
Model:
NDC# 41595-5513-2
UPC Codes:
883484717943
Lot Numbers:
19277K2
19278K1

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84620
Status: Resolved
Manufacturer: Idelle Labs
Manufactured In: Canada, United States
Units Affected: 4 products (Unknown; Unknown; Unknown; Unknown)
Distributed To: Nationwide
Agency Last Updated: January 16, 2020

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 ยท 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.