Recalls / Class I
Class IF-0924-2022
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-1 22oz. plastic jar and 34 oz. can. 6 units per case. Item numbers: 6499213 6698213 Retail UPCs: 055325000808 055325001638
- Type
- Food
- Affected lot / code info
- Batches: 28091SH00 35007SH00 24493SH00 26773SH00 27992SH00 28174SH00 31495SH00 34815SH00 36099SH00 37294SH00
- Quantity
- 54507 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-0924-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings.