Abbott Similac Pro-Sensitive Infant Formula with Iron 20.1oz
Food recall F-0930-2022. Published in FDA’s Enforcement Report on Mar 16, 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 Mar 16, 2022. Copied from openFDA on Oct 20, 2026.
- Class I FDA’s most serious class (needs attention)
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 938215 cases 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?
Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Abbott Similac Pro-Sensitive Infant Formula with Iron 20.1oz. and 22.5oz. plastic jar. 4 jars per case; 34oz. plastic jar. 6 jars per case; 7oz. can. 6 cans per case. Item numbers: 66084 66657 67923 68090 Retail UPCs: 070074660820 070074666587 070074679242 070074680910
938215 cases, in FDA’s words.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Batches: 23421SH00 24509SH00 24510SH00 24567SH00 24568SH00 25589SH00 25590SH00 25689SH00 26740SH00 26742SH00 26744SH00 24452SH00 24453SH00 24507SH00 24508SH00 25573SH00 25574SH00 25576SH00 25648SH00 25649SH00 26746SH00 26790SH00 26822SH00…
Every code shown here, 978 characters
Batches: 23421SH00 24509SH00 24510SH00 24567SH00 24568SH00 25589SH00 25590SH00 25689SH00 26740SH00 26742SH00 26744SH00 24452SH00 24453SH00 24507SH00 24508SH00 25573SH00 25574SH00 25576SH00 25648SH00 25649SH00 26746SH00 26790SH00 26822SH00 26823SH00 27876SH00 27877SH00 29201SH00 29202SH00 29203SH00 29204SH01 29218SH00 29218SH01 29233SH00 29298SH00 29299SH00 30336SH00 31455SH00 31456SH00 31499SH00 31500SH00 32636SH00 32638SH00 33731SH00 33732SH00 33734SH00 34802SH00 34804SH00 35037SH00 35038SH00 35047SH00 35048SH00 35979SH00 35980SH00 35992SH00 35993SH00 36186SH00 36187SH00 36188SH00 36199SH00 36200SH00 25575K800 27953K800 27955K800 28023K800 28175K800 28176K800 29241K800 30320K800 30321K800 30337K800 31458K800 31589K800 33716K800 33733K800 27979SH00 27980SH00 27981SH00 28102SH00 28102SH10 28154SH00 28155SH00 28155SH01 28177SH00 29231SH00 29232SH00 30443SH00 30445SH00 31453SH00 32639SH00 35009SH00 35010SH00 35053SH00 35054SH00 35078SH00 35079SH00 35080SH00 36216SH00
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US Nationwide. Worldwide.
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.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 Feb 17, 2022.
- FDA classified it on Mar 30, 2022.
- FDA’s Enforcement Report published it on Mar 16, 2022.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Abbott Laboratories, of Abbott Park, IL.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Press Release.
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
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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.