FDA Recall United States Terminated Historical recordClass II
MOTTS LLP
- Product
- Motts No Sugar Added Apple Sauce - 3.9 oz.
- Published
- December 8, 2021
- Distribution
- IL
MOTTS LLP Recall: Elevated patulin levels
United States
TerminatedClass II
- Company
- MOTTS LLP
- Product
- Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Contai…
- Recall date
- May 18, 2023
- Terminated
- November 21, 2024
- Source
- FDA
Reason for recall
Elevated patulin levels
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Containers 23.4 oz (666g). Individual units are packaged in plastic cups and placed in a cardboard sleeve of 6 sups with 12 sleeves to a case. Retail unit UPC is 14800000078 . Case label UPC is 10014800000075 | Not published in this source record | 9,593 cases | 042123LYtt:tt / Best By: AUG 13 24 and 042223LYttt:tt / Best By: AUG 14 24 |
Distribution
- US states including: AL
- CT
- FL
- GA
- IA
- IL
- IN
- KY
- MA
- MD
- ME
- MI
- MN
- MO
- NC
- NJ
- NY
- OH
- PA
- SC
- TN
- TX
- VA
- WI; Bermuda and Dominican Republic
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1016-2023
- Event ID
- 92384
- Status
- Terminated
- Classification
- Class II
- Company
- MOTTS LLP
- Product description
- Mott s no sugar added applesauce 6 pack 3.9 oz (111g) Containers 23.4 oz (666g). Individual units are packaged in plastic cups and placed in a cardboard sleeve of 6 sups with 12 sleeves to a case. Retail unit UPC is 14800000078 . Case label UPC is 10014800000075
- Quantity
- 9,593 cases
- Reason
- Elevated patulin levels
- Recall initiation date
- May 18, 2023
- Report date
- July 5, 2023
- Classification date
- Not published in this source record
- Termination date
- November 21, 2024
- Distribution pattern
- US states including: AL, CT, FL, GA, IA, IL, IN, KY, MA, MD, ME, MI, MN, MO, NC, NJ, NY, OH, PA, SC, TN, TX, VA, WI; Bermuda and Dominican Republic
- UPC, lot, and code information
- 042123LYtt:tt / Best By: AUG 13 24 and 042223LYttt:tt / Best By: AUG 14 24
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: MOTTS LLP
Other recalls from MOTTS LLP
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 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kentucky | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| New Jersey | 1 |
| New York | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Virginia | 1 |
| Wisconsin | 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.
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