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Similac 360 Total Care 2 fl oz reclose able plastic bottle Packaged as: 6 count carton, 12 count carton, 48 count case

Class I - Dangerous
Recalled: October 13, 2022 Abbott Laboratories Other Foods

What Should You Do?

  1. Check if you have this product:
    Batch No. 35609N200, 39480N200, 39633N200, 40624N200, 40715N200, 40738N200, 41001N200, 377777N200, 41756N200, 41793N200, 41875N200, 40716N200, 37778N200, 40755N200, 4296N200, 41754N200, 40755N200, 38779N200, 40755N200 Case No. 38493XK00, 39480N200, 39633N200, 40624N200, 40715N200, 41001N200, 41543XK00, 41756N200, 41793N200, 41875N200, 420258H00, 42564XK00, 42566XK00, 42567XK00, 42568XK00, 42572XK00, 42573XK00, 42962N200, 430264R00, 43579XK00, 43580XK00, 43581XK00, 440324R00, 450394R00 Product No. 68133, 68136, 68708, 68133 Best By 12/01/22, 02/01/23, 03/01/23, 04/01/23, 05/01/23, 06/01/23, 07/01/23
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Abbott Laboratories
Reason for Recall:
Compromised seal integrity which could lead to spoilage
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Similac 360 Total Care 2 fl oz reclose able plastic bottle Packaged as: 6 count carton, 12 count carton, 48 count case

Product Codes/Lot Numbers:

Batch No. 35609N200, 39480N200, 39633N200, 40624N200, 40715N200, 40738N200, 41001N200, 377777N200, 41756N200, 41793N200, 41875N200, 40716N200, 37778N200, 40755N200, 4296N200, 41754N200, 40755N200, 38779N200, 40755N200 Case No. 38493XK00, 39480N200, 39633N200, 40624N200, 40715N200, 41001N200, 41543XK00, 41756N200, 41793N200, 41875N200, 420258H00, 42564XK00, 42566XK00, 42567XK00, 42568XK00, 42572XK00, 42573XK00, 42962N200, 430264R00, 43579XK00, 43580XK00, 43581XK00, 440324R00, 450394R00 Product No. 68133, 68136, 68708, 68133 Best By 12/01/22, 02/01/23, 03/01/23, 04/01/23, 05/01/23, 06/01/23, 07/01/23

Distribution:

Distributed in: DC

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0156-2023

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