CLASS I Food recall · Reported 7 Sep 2022 · FDA Enforcement Report

Prouct Was Not recalled by Lyons Magnus

Lyons Magnus is recalling Prouct Was Not, distributed nationwide in the US. The recall was initiated on 22 Jul 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesEXPANDED 8-10-2022 Lot Code 1102 / Best By Date 2023.01.11 Lot Code 2031 / Best By Date 2022.10.29 Lot Code 3031 / Best By Date 2022.10.30 Lot Code 4031 / Best By Date 2022.10.31 Lot Code 5031 / Best By Date 2022.11.01 Lot Code 5231 / Best By Date 2022.11.21 Lot Code 6231 / Best By Date 2022.11.21 Lot Code 7402 / Best By Date 2023.02.16 Lot Code 7521 / Best By Date 2022.09.14 Lot Code 7531 / Best By Date 2022.12.23 Lot Code 8521 / Best By Date 2022.09.15 Lot Code 8531 / Best By Date 2022.12.24
Quantity recalled53,818,025 total units

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-1676-2022
FDA event ID
90667
Recalling firm
Lyons Magnus, Fresno, CA
Classification
Class I
Status
Terminated
Recall initiated
22 Jul 2022
FDA classified
30 Aug 2022
Reported
7 Sep 2022
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Botulism
Product category
Other

Timeline

22 Jul 2022Recall initiated by company
30 Aug 2022Classified by FDA+39 days
7 Sep 2022Published 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

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Product as listed by the FDA

PROUCT WAS NOT DISTRIBUTED IN US. The Original Oatly! Oat Drink Deluxe 330ml. UPC 7 394376 619021 18 count case UPC 27394376619025. Shake well before drinking. Produced in the USA. Oatly AB, Stora Varvsgatan 6a, SE-211 19 Malmo.

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Prouct Was Not recalled?

Yes. Lyons Magnus recalled Prouct Was Not on 22 Jul 2022. The recall is Class I and its status is Terminated. Recall number F-1676-2022.

Why was it recalled?

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Which lots are affected?

EXPANDED 8-10-2022 Lot Code 1102 / Best By Date 2023.01.11 Lot Code 2031 / Best By Date 2022.10.29 Lot Code 3031 / Best By Date 2022.10.30 Lot Code 4031 / Best By Date 2022.10.31 Lot Code 5031 / Best By Date 2022.11.01 Lot Code 5231 / Best By Date 2022.11.21 Lot Code 6231 / Best By Date 2022.11.21 Lot Code 7402 / Best By Date 2023.02.16 Lot Code 7521 / Best By Date 2022.09.14 Lot Code 7531 / Best By Date 2022.12.23 Lot Code 8521 / Best By Date 2022.09.15 Lot Code 8531 / Best By Date 2022.12.24

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 21 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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