CLASS II Food recall · Reported 22 Sep 2021 · FDA Enforcement Report

Albanese World's Best Mini Gummi Butterflies recalled

Albanese Confectionery Group is recalling Albanese World's Best Mini Gummi Butterflies, distributed in Michigan, Oklahoma. The recall was initiated on 18 Aug 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 1202011130
Quantity recalled226 cases (12 retail units per case)

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-0984-2021
FDA event ID
88587
Recalling firm
Albanese Confectionery Group, Merrillville, IN
Classification
Class II
Status
Terminated
Recall initiated
18 Aug 2021
FDA classified
16 Sep 2021
Reported
22 Sep 2021
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Other Reasons
Product category
Other

Timeline

18 Aug 2021Recall initiated by company
16 Sep 2021Classified by FDA+29 days
22 Sep 2021Published 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

Product contains comingled Olly Sleep dietary supplement which may cause drowsiness

Product as listed by the FDA

Albanese World's Best Mini Gummi Butterflies 7.5oz UPC 634418523525

Where it was distributed

Distributors in OK and MI for further distribution to retail stores

MichiganOklahoma

Questions about this recall

Why was it recalled?

Product contains comingled Olly Sleep dietary supplement which may cause drowsiness

Which lots are affected?

Lot: 1202011130

Where was it sold?

Distributors in OK and MI for further distribution to retail stores

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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.

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