Fresh Recalls

FDAClass II · Food · Recall H-1154-2026 · Recalled July 22, 2026

Pillsbury Bread Rolls recall — General Mills James Ford Bell Technical Center

Agency report date: July 22, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Pillsbury Bread Rolls
Company / brand
General Mills James Ford Bell Technical Center
Lot / serial / date codes
Better if Used by OCT 12 26 / Lot: 11JUN6JL Better if Used by OCT 13 26 / Lot: 12JUN6JL
Distribution
AR, CA, FL, GA, IN, LA, ME, MO, NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, WY
Agency product description and boundaries

Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC 107-21582-13283-1. Keep Frozen. Case Qty 180. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Potential foreign material (glass)

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Pillsbury Bread Rolls

3. Open the official notice or contact

Official recall ID
H-1154-2026
Brand
General Mills James Ford Bell Technical Center
Classification
Class II
Units affected
3080 cases
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Golden Valley, MN, United States
Firm address
9000 Plymouth Ave N, 55427-3870

Identifying details (verbatim from the notice)

Product codes / lots
Better if Used by OCT 12 26 / Lot: 11JUN6JL Better if Used by OCT 13 26 / Lot: 12JUN6JL
Distribution
AR, CA, FL, GA, IN, LA, ME, MO, NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, WY
Firm notified the public via
E-Mail
FDA event ID
99293
Recall initiated
June 19, 2026
FDA classified
July 13, 2026
FDA report date
July 22, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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