The Original Oatly! Oat-Milk 11 fl oz
Food recall F-1675-2022. Published in FDA’s Enforcement Report on Sep 7, 2022.
- FDA Class I
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Sep 7, 2022. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 53,818,025 total units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class I, the most serious of FDA’s three classes.
“Dangerous or defective products that predictably could cause serious health problems or death. Examples include: food found to contain botulinum toxin, food with undeclared allergens, a label mix-up on a lifesaving drug, or a defective artificial heart valve.”
openFDA, in plain words, its enforcement report fields.
“Class I is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”
FDA’s rule, 21 CFR 7.3(m)(1), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
The Original Oatly! Oat-Milk 11 fl oz (330ml). UPC 1 90646-63013 3. 18 count case UPC 20190646630137. Distributed by Oatly Inc., 220 E 42ndSt., Ste. 409A, New York, NY 10017.
53,818,025 total units, in FDA’s words.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
EXPANDED 8-10-2022 Lot Code 1202 / Best By Date 21Jan2023 LM Lot Code 2202 / Best By Date 22Jan2023 LM Lot Code 3231 / Best By Date 19Nov2022 LM Lot Code 4102 / Best By Date 14Jan2023 LM Lot Code 4231 / Best By Date 20Nov2022 LM Lot Code…
Every code shown here, 480 characters
EXPANDED 8-10-2022 Lot Code 1202 / Best By Date 21Jan2023 LM Lot Code 2202 / Best By Date 22Jan2023 LM Lot Code 3231 / Best By Date 19Nov2022 LM Lot Code 4102 / Best By Date 14Jan2023 LM Lot Code 4231 / Best By Date 20Nov2022 LM Lot Code 4531 / Best By Date 20Dec2022 LM Lot Code 5231 / Best By Date 21Nov2022 LM Lot Code 5531 / Best By Date 21Dec2022 LM Lot Code 6402 / Best By Date 15Feb2023 LM Lot Code 7802 / Best By Date 28Mar2023 LM Lot Code 8802 / Best By Date 29Mar2023 LM
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Barcodes and drug codes
-
UPC
190646630133 -
UPC
20190646630137
As FDA’s description and codes give them; the UPCs written as digits only.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Nationwide
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jul 22, 2022.
- FDA classified it on Aug 30, 2022.
- FDA’s Enforcement Report published it on Sep 7, 2022.
- FDA terminated it on Jul 25, 2024.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Lyons Magnus, Inc, of Fresno, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Telephone.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- Meat, poultry and egg products are recalled by USDA’s Food Safety and Inspection Service, not FDA, and its recalls aren’t here yet: see fsis.usda.gov.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Food recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.