Recalls / Class I
Class IF-0925-2022
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 Advance Step-2 22.5oz. plastic jar. 6 jars per case. Abbott Similac Advance 34oz. can. 6 cans per case. Abbott Similac Pro-Advance 20.6oz. and 859g. plastic jar. 6 jars per case. Item numbers: 6499113 6698313 6818113 6818313 Retail UPCs: 055325000808 055325001645 055325002864 055325002888
- Type
- Food
- Affected lot / code info
- Batches: 27887SH00 31497SH00 35006SH00 23411SH00 25587SH00 26774SH00 27993SH00 28087SH00 29186SH00 30315SH00 31465SH00 31496SH00 35996SH00 36120SH10 36295SH10 32642SH00 35058SH10 35058SH00 36348SH00 37297SH00
- Quantity
- 103025 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-0925-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings.