FDA Recall United States OngoingHistorical recordClass I
Abbott Laboratories
- Product
- Abbott Similac PM 60/40 Low Iron Infant Formula, 14.1oz. can…
- Published
- March 16, 2022
- Distribution
- Nationwide
United States
OngoingClass I
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
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Abbott EleCare Junior Vanilla 14.1oz. can and Abbott EleCare Jr Similac Vanilla 14.1oz. can. 6 cans per case. Item numbers: 56585 5658557 Retail UPCs: 070074565866 070074116723 | Not published in this source record | 116350 cases | Batches: 24531Z200 26722Z200 26808Z200 26859Z200 28128Z200 28139Z200 28140Z200 30391Z200 34772Z200 34934Z200 36147Z200 24531Z201 28128Z201 30391Z201 34772Z201 36147Z201 |
This recall shares FDA event ID 89629 with 10 other product entries in Public Health Trace.
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
FDA Recall United States OngoingHistorical recordClass I
Responsible company: Abbott Laboratories
FDA Recall United States TerminatedTerminated: September 3, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: December 14, 2023Historical recordClass II
FDA Recall United States TerminatedTerminated: August 14, 2024Historical recordClass II
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Retrieved by Public Health Trace:
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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Public Health Trace last retrieved this record on July 18, 2026.
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