CLASS I ONGOING Food recall · Reported 3 Jun 2026 · FDA Enforcement Report

Butter Parsley Bagel Crisps recalled by Legacy Bakehouse

Legacy Bakehouse is recalling Butter Parsley Bagel Crisps, distributed in Pennsylvania, Wisconsin. The recall was initiated on 5 May 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # / Production Date: 29 JAN 2026 and 12 APR 2026
Quantity recalled750 - 10 lb. 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
H-0850-2026
FDA event ID
98928
Recalling firm
Legacy Bakehouse, Waukesha, WI
Classification
Class I
Status
Ongoing
Recall initiated
5 May 2026
FDA classified
26 May 2026
Reported
3 Jun 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Salmonella
Product category
Bread

Timeline

5 May 2026Recall initiated by company
26 May 2026Classified by FDA+21 days
3 Jun 2026Published in enforcement report+8 days

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

Reason for recall

Products were made with recalled California Dairies milk powder due to Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Butter Parsley Bagel Crisps, Item Number 18490, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Waukesha, WI 53166.

Where it was distributed

PA, WI

PennsylvaniaWisconsin

Questions about this recall

Why was it recalled?

Products were made with recalled California Dairies milk powder due to Salmonella.

Which lots are affected?

Lot # / Production Date: 29 JAN 2026 and 12 APR 2026

Where was it sold?

PA, WI

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.

Other products in this recall event

2 other products · FDA event 98928

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