CLASS I Food recall · Reported 16 Apr 2025 · FDA Enforcement Report

365 Whole Foods Market Small Bites Macaroni & Cheese recalled

C.H. Guenther & Son is recalling 365 Whole Foods Market Small Bites Macaroni & Cheese, distributed nationwide in the US. The recall was initiated on 11 Mar 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest-By Date: 11/29/25
Quantity recalled1818 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0702-2025
FDA event ID
96513
Recalling firm
C.H. Guenther & Son, San Antonio, TX
Classification
Class I
Status
Terminated
Recall initiated
11 Mar 2025
FDA classified
10 Apr 2025
Reported
16 Apr 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Herbal Supplements

Timeline

11 Mar 2025Recall initiated by company
10 Apr 2025Classified by FDA+30 days
16 Apr 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared allergen (eggs) and pork

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482499709. Distributed by: Whole Foods Market, Austin, TX

Where it was distributed

Nationwide

Nationwide

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Undeclared allergen (eggs) and pork

Which lots are affected?

Best-By Date: 11/29/25

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from C.H. Guenther & Son

All 84

Other Herbal Supplements recalls

All 509