Food/Recall·FDA Recalls, Market Withdrawals & Safety Alerts

My Wife’s Slaw Issues a Voluntary Recall of its Original and Jalapeno Heat Flavored Coleslaw for Being Adulterated

MediumPublished May 5, 2026· AI-analyzed May 10, 2026View original FDA source
AI-generated regulatory interpretation. The four sections below are an analyst-style summary produced by an AI model from the original FDA source. Always verify against the source before any regulatory, clinical, or commercial decision.
What happened

My Wife’s Slaw has issued a voluntary recall for its Original and Jalapeno Heat flavored coleslaw in 8 oz and 16 oz glass jars due to being produced without inspection. The source notes the products are considered adulterated because they lacked appropriate inspection and verification of safety parameters.

Who it affects

This recall affects My Wife's Slaw, retailers carrying their 8 oz and 16 oz products, and QA/manufacturing professionals responsible for food inspection compliance.

Why it matters

The classification of 'adulterated' due to lack of inspection suggests a significant break in the regulatory oversight process during manufacturing. For regulatory teams, this highlights that even if no specific pathogen is identified, the absence of documented safety parameters and formal inspection oversight is sufficient to trigger a voluntary recall of refrigerated products.

Practical takeaway

Quality teams should immediately verify that all facility registrations and retail certifications are current. Production managers should audit batch records to ensure all listed safety parameters were monitored and documented according to standard Operating Procedures.

FDA source material

Zanesville, Ohio (May 5, 2026) - My Wife’s Slaw is voluntarily recalling its Original and Jalapeno Heat flavored coleslaw sold in 8 oz and 16 oz glass mason jars. The products included in this recall are adulterated because they were produced without the benefit of inspection and the safety paramete

Open in openFDA / FDA.gov
AI-generated interpretation. Always verify critical decisions against the original FDA source. Generated with google/gemini-3-flash-preview.