FDA Recall United States Terminated Historical recordClass II
Abbott Laboratories
- Product
- Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in fo…
- Published
- November 15, 2023
- Distribution
- Alabama, Arkansas, Arizona, California,…
Abbott Laboratories Recall: Potential of foreign material (hard plastic) within product
United States
TerminatedClass II
- Company
- Abbott Laboratories
- Product
- Zone Perfect Fudge Graham bar 50g bars packaged in foil wrap…
- Recall date
- March 28, 2023
- Terminated
- December 14, 2023
- Source
- FDA
Reason for recall
Potential of foreign material (hard plastic) within product
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton | Not published in this source record | 646,668 bars | Lot No - 47961B800 List No - 63259 Expiration Date 03/01/24 Display Lot No - 49012SQoo Display List No - 64138 |
Distribution
- AL
- AZ
- CA
- CO
- CT
- FL
- GA
- IA
- ID
- IL
- IN
- KS
- LA
- MA
- MD
- ME
- MI
- MN
- MO
- NC
- NE
- NJ
- NV
- NY
- OH
- PA
- SC
- SD
- TN
- TX
- UT
- VA
- WA
- WI
- WV
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0698-2023
- Event ID
- 92015
- Status
- Terminated
- Classification
- Class II
- Company
- Abbott Laboratories
- Product description
- Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton
- Quantity
- 646,668 bars
- Reason
- Potential of foreign material (hard plastic) within product
- Recall initiation date
- March 28, 2023
- Report date
- April 19, 2023
- Classification date
- Not published in this source record
- Termination date
- December 14, 2023
- Distribution pattern
- AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NV, NY, OH, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV
- UPC, lot, and code information
- Lot No - 47961B800 List No - 63259 Expiration Date 03/01/24 Display Lot No - 49012SQoo Display List No - 64138
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Abbott Laboratories
Other recalls from Abbott Laboratories
FDA Recall United States Terminated Historical recordClass II
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- Product
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- Published
- November 23, 2022
- Distribution
- Domestic: Alaska, Alabama, Arizona, Cali…
FDA Recall United States Terminated Historical recordClass II
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- Product
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- Published
- November 23, 2022
- Distribution
- Domestic: Alaska, Alabama, Arizona, Cali…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alabama | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| New Jersey | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| South Dakota | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| West Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
