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Class IFDA · July 1, 2026

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate recall

Recalled by Spring & Mulberry Inc.

The product, as the FDA describes it: Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Why it was recalled

Potential Salmonella contamination

What to do if you have it

Nothing about spring & mulberry mixed berry date-sweetened chocolate will look or smell wrong, because the organisms behind this kind of recall leave no trace you can see or taste. Do not cook it to make it safe and do not sample it. Throw it out or return it, then wash anything it touched, including the shelf it sat on and the container beside it.

How to tell whether your package is one of them

A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.

Product Number SMBARMB20001 Batch/Lot 025220 and Use By 08/31/2026 Batch/Lot 025223 and Use By 08/31/2026 Batch/Lot 025247 and Use By 09/30/2026 Batch/Lot 025248 and Use By 09/30/2026 Batch/Lot 025251 and Use By 09/30/2026 Batch/Lot 025253 and Use By 09/30/2026 Batch/Lot 025275 and Use By 10/31/2026 Batch/Lot 025281 and Use By 10/31/2026 Batch/Lot 025288 and Use By 10/31/2026 Batch/Lot 025296 and Use By 10/31/2026 Batch/Lot 025335 and Use By 12/31/2026 Batch/Lot 025337 and Use By 12/31/2026 Batch/Lot 026008 and Use By 01/31/2027

The details on record

Recalling companySpring & Mulberry Inc.
Company locationRaleigh, NC
Where it was distributedNationwide
How much was recalled66,779 individual bars
Recall startedJanuary 9, 2026
Published by the FDAJuly 1, 2026
Recall typeVoluntary: Firm initiated
How the company announced itTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA recall numberH-1097-2026

Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.

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