Laura Lynn Foaming Pear Hand Soap Lawsuit Update: Injuries, Recall Status, and Legal Options

Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers has been recalled because of potential bacterial contamination, according to U.S. Food and Drug Administration enforcement records. The recall covers 294 cases of 7.5-fluid-ounce bottles distributed by Ingles Markets, including lot 26-01001 with a best-by date of March 13, 2028.
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Collen Clark Published by Collen Clark

The voluntary recall was initiated in June 2026 and later classified by the FDA as Class II, meaning exposure could cause temporary or medically reversible adverse health consequences while the probability of serious consequences is considered remote. Consumers should identify affected bottles by the product name, UPC, lot code, and best-by date.

Quick Facts

  • Product: Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers
  • Amount recalled: 294 cases of 7.5-fluid-ounce bottles
  • Hazard: Potential bacterial contamination
  • Identification: Lot 26-01001; best-by date March 13, 2028

Latest Laura Lynn Foaming Pear Hand Soap Recall Developments

September 2026

September 11, 2026 – The FDA classified the broader Intercon Chemical Co. hand soap recall as Class II. FDA defines a Class II recall as one in which exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse consequences is remote. [1]

September 2026 – FDA enforcement information identified Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers as recall C-0018-2026. The affected product is the 7.5-fluid-ounce bottle with UPC 08685407408, manufacturing code FIN46-HB-12X7-0948, lot code 26-01001, and a best-by date of March 13, 2028.

June 2026

June 29, 2026 – Intercon Chemical Co. initiated a voluntary recall involving six hand soap products because of potential bacterial contamination. The broader action included two Laura Lynn soaps distributed by Ingles Markets along with Intercon, Clearly Better, Summit 150, and Vestis products.

What Is the Laura Lynn Foaming Pear Hand Soap Recall?

The recall involves Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers distributed by Ingles Markets Inc. of Asheville, North Carolina. The affected product was packaged in 7.5-fluid-ounce containers.

FDA enforcement information lists 294 cases of the Laura Lynn Foaming Pear soap as recalled. The product is associated with recall number C-0018-2026.

The Laura Lynn soap was one of six hand soap products included in a broader voluntary recall initiated by Intercon Chemical Co. The products were distributed through wholesalers and retail channels across multiple states.

How Can Consumers Identify the Recalled Laura Lynn Soap?

Consumers should check the information printed on the bottle rather than relying only on the Laura Lynn brand or pear scent. The recalled product is identified by the following information:

  • Product: Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers
  • Size: 7.5 fluid ounces
  • UPC: 08685407408
  • Manufacturing code: FIN46-HB-12X7-0948
  • Lot code: 26-01001
  • Best-by date: March 13, 2028
  • Recall number: C-0018-2026
  • Quantity: 294 cases

The long shelf life is significant because affected bottles may remain in homes, storage areas, or supply cabinets well after the recall was initiated.

Why Was Laura Lynn Foaming Pear Hand Soap Recalled?

The FDA enforcement record lists the reason for the Laura Lynn recall as potential bacterial contamination. The publicly available record does not identify a specific bacterial species for this particular Laura Lynn product.

That distinction is important because two Intercon-branded soaps included in the broader recall were specifically associated with potential contamination by several Pseudomonas and Serratia species. The FDA record does not state that those same organisms were found in the recalled Laura Lynn Foaming Pear soap.

The Laura Lynn product therefore should be described as potentially contaminated with bacteria rather than as confirmed to contain a particular organism.

What Other Hand Soaps Were Included in the Recall?

The broader Intercon Chemical recall included six products:

The second Laura Lynn product, Honey Apple Crisp Liquid Hand Soap, was recalled in 301 cases. Together, FDA records list 595 cases of the two Laura Lynn products.

What Does a Class II FDA Recall Mean?

The FDA classifies recalls according to the degree of potential health risk. A Class II recall applies when exposure may cause temporary or medically reversible adverse health effects, or when the likelihood of serious adverse health consequences is considered remote. [1]

A Class II classification does not mean that every person who used the recalled soap will become ill. It indicates that FDA determined the circumstances warranted removal of the potentially contaminated product from distribution.

Can Contaminated Hand Soap Cause an Infection?

Bacterial contamination of a personal-care product can potentially expose users when the product contacts the skin, cuts, wounds, eyes, or other vulnerable areas. The actual health risk depends on the organism involved, the level of contamination, the route of exposure, and the health of the individual.

People with open wounds or compromised immune defenses may be more vulnerable to certain opportunistic bacteria. For example, the Centers for Disease Control and Prevention notes that people with open wounds, medical devices, or ventilators are among those at increased risk of Pseudomonas aeruginosa infection. [2]

However, the FDA record does not specifically state that Pseudomonas aeruginosa contaminated the Laura Lynn Foaming Pear product. That organism was identified in connection with certain other soaps in the broader recall.

Who May Be Affected?

Consumers who purchased Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers should check the bottle for lot code 26-01001 and the March 13, 2028 best-by date. Matching bottles fall within the FDA enforcement record for the recall.

Consumers who developed a diagnosed infection, significant skin reaction, or another medical problem after using a recalled bottle may want to preserve the soap container, lot information, purchase records, photographs, medical records, and laboratory test results.

What Should Consumers Do With Recalled Laura Lynn Hand Soap?

Consumers with an affected bottle should stop using the recalled product. The product name, bottle size, UPC, lot code, and best-by date should be checked carefully against the recall information.

Anyone experiencing symptoms of an infection or another concerning reaction after using a recalled product should contact a healthcare professional. The diagnosis and any laboratory testing may also be relevant if the consumer later seeks an individual legal review.

Have Illnesses Been Reported?

Publicly available reporting reviewed for this article does not identify confirmed illnesses associated specifically with the recalled Laura Lynn Foaming Pear Scent Hand Soap. The recall was initiated because of potential bacterial contamination rather than a publicly reported outbreak of infections.

The absence of reported illnesses does not establish that an affected bottle is safe to continue using. Recall status is based on the product and lot information identified in the FDA enforcement record.

Who May Be Liable for a Contaminated Hand Soap Injury?

Potential liability depends on the circumstances of an individual case and applicable state law. Manufacturers, distributors, retailers, or other companies involved in producing and supplying an allegedly contaminated consumer product may potentially be evaluated if exposure causes an injury.

Potential legal theories may include manufacturing defects, negligence, breach of warranty, or failure to adequately respond to contamination risks. A consumer generally must establish that the product was contaminated or otherwise defective and that exposure caused or contributed to the claimed injury.

Ingles Markets Inc. is identified as the distributor of the recalled Laura Lynn product. The existence of an FDA recall alone does not establish legal liability in an individual case.

Current Laura Lynn Foaming Pear Hand Soap Lawsuit Status

The FDA records document a Class II product recall involving the Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers. The federal recall information does not itself announce a class action, multidistrict litigation proceeding, personal injury settlement, or coordinated compensation program for consumers.

An individual product-liability claim may still be evaluated if a consumer allegedly developed a medically documented infection or other significant injury after exposure to an affected bottle. Whether a claim is viable depends on product identification, medical evidence, causation, damages, and applicable law.

Do I Qualify for a Laura Lynn Hand Soap Claim?

  • Did you use Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers from recalled lot 26-01001?
  • Did the bottle have a March 13, 2028 best-by date?
  • Did you develop a diagnosed infection, significant skin reaction, or other illness after using the product?
  • Do you have medical records, laboratory results, photographs, or the recalled bottle?

Answering yes to one or more questions does not automatically establish a lawsuit. An attorney can review the recalled product, exposure history, medical evidence, laboratory findings, and applicable filing deadlines to determine whether additional investigation may be appropriate.

  1. Free case review. An attorney reviews the recalled soap, exposure history, symptoms, and medical diagnosis.
  2. Investigation. Evidence may include the bottle, lot code, photographs, purchase records, medical records, laboratory test results, and FDA recall information.
  3. Filing. If the available evidence and applicable law support a claim, a product-liability lawsuit may be filed against one or more potentially responsible parties.
  4. Discovery/negotiation. The parties may exchange records, obtain testimony, retain experts, evaluate causation, and discuss possible resolution.
  5. Resolution. A claim may conclude through settlement, dismissal, court ruling, or trial depending on its facts and procedural history.

Compensation in a Contaminated Hand Soap Case

Depending on the circumstances, a consumer who develops a medically documented illness may seek damages for medical expenses, lost income, pain and suffering, and other losses recognized under applicable law. Available damages depend on the severity of the illness, evidence of causation, and jurisdiction.

Compensation amounts vary by case. Past results do not guarantee future outcomes.

Important Laura Lynn Hand Soap Recall Developments

Event Month/Year Type Status Source Notes
FDA Class II Classification September 2026 FDA Recall Classification Class II [1] Temporary or reversible effects possible
Laura Lynn Foaming Pear Recall June 2026 Voluntary Product Recall Recalled [3] 294 cases affected
Intercon Hand Soap Recall Initiated June 2026 Voluntary Recall Initiated [3] Six soap products included

Frequently Asked Questions

What is the Laura Lynn Foaming Pear Hand Soap Recall Lawsuit?

The Laura Lynn Foaming Pear Hand Soap Recall Lawsuit topic concerns potential individual claims involving recalled hand soap associated with potential bacterial contamination. FDA enforcement records identify 294 cases of the affected 7.5-fluid-ounce product.

Which Laura Lynn Foaming Pear soap was recalled?

The recall covers 7.5-fluid-ounce Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers with UPC 08685407408. The affected lot is 26-01001 with a best-by date of March 13, 2028.

Why was the Laura Lynn soap recalled?

The FDA enforcement record lists the reason as potential bacterial contamination. The record does not identify a specific bacterial species for this Laura Lynn product.

Does the Laura Lynn soap contain Pseudomonas or Serratia bacteria?

The FDA specifically identified Pseudomonas and Serratia species in connection with two Intercon-branded soaps in the broader recall. Public FDA recall information does not state that those same bacteria were identified in the Laura Lynn Foaming Pear soap.

How much Laura Lynn Foaming Pear soap was recalled?

FDA enforcement information lists 294 cases of the 7.5-fluid-ounce Laura Lynn Foaming Pear product. The recall number is C-0018-2026.

What does FDA Class II mean?

A Class II recall means exposure may cause temporary or medically reversible adverse health consequences, or that the probability of serious consequences is remote. It is a lower risk classification than a Class I recall.

Have any infections been reported?

No confirmed infections specifically linked to the Laura Lynn Foaming Pear soap were identified in the public recall information reviewed for this article. Consumers should nevertheless stop using bottles that match the recalled lot information.

Can I file a Laura Lynn Foaming Pear Hand Soap Recall Lawsuit?

A consumer who developed a medically documented infection or significant injury allegedly associated with an affected bottle may warrant an individual legal review. A recall alone does not establish liability, and any claim depends on product identification, exposure, causation, medical evidence, damages, and applicable law.

Do I Have a Laura Lynn Foaming Pear Hand Soap Lawsuit?

If you or a loved one developed a serious infection or other significant injury after using recalled Laura Lynn Foaming Pear Scent Hand Soap with Moisturizers, you may have legal options. Contact Schmidt & Clark for a free case review.

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References

[1] https://www.fda.gov/safety/industry-guidance-recalls/recalls-background-and-definitions

[2] https://www.cdc.gov/pseudomonas-aeruginosa/about/index.html

[3] https://www.fda.gov/about-fda/open-government-fda-data-sets/recalls-data-sets

[4] https://828newsnow.com/news/228822-fda-recall-includes-2-laura-lynn-hand-soaps-from-ingles/

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