Recalls / Class I
Class IF-0933-2022
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Abbott Similac Pro-Advance 20.6oz., 30.3oz., 34oz., and 658g plastic jar. 6 jars per case. 7oz. can. 6 cans per case. Item numbers: 6720113 6720813 6726613 6818013 6818213 6832313 Retail UPCs: 055325002499 055325002543 055325002604 055325002819 055325002833 055325003069
- Type
- Food
- Affected lot / code info
- Batches: 32624SH00 34958SH00 25673SH00 31463SH00 31549SH00 32625SH00 32626SH00 25604K800 31454K800 35008K800 37251K800 35055SH00 35056SH00 32624SH01 32625SH01 32626SH01
- Quantity
- 135652 cases
Why it was recalled
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
Recalling firm
- Firm
- Abbott Laboratories
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 100 Abbott Park Rd Bldg Ap8b, N/A, Abbott Park, Illinois 60064-3502
Distribution
- Distribution pattern
- US Nationwide. Worldwide.
Timeline
- Recall initiated
- 2022-02-17
- FDA classified
- 2022-03-30
- Posted by FDA
- 2022-03-16
- Status
- Ongoing
Source: openFDA Food Enforcement endpoint. Recall record F-0933-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings.