Manicaretti Inc Recall: Rapid Alert System for Food and Feed notification received from Italy regarding high histamine levels in imported anchovy sauce.
United States
TerminatedClass II
- Company
- Manicaretti Inc
- Product
- IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT; 100 ml a…
- Recall date
- January 12, 2018
- Terminated
- May 8, 2018
- Source
- FDA
Reason for recall
Rapid Alert System for Food and Feed notification received from Italy regarding high histamine levels in imported anchovy sauce.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT; 100 ml and 250 ml sizes; UPC 100 ml - 7 93232 54200 3; UPC 250 ml - 7 93232 54203 4 Ingredients: Anchovies, Salt, Water. Product of Italy. Produced by ISA srl Pellezzano (SA) | Not published in this source record | 811 CS FOR 100ML AND 101 CS FOR 250ML (6 units per case) | 100ML L.11/2015 EXP:11/30/2018 L.08/2016 EXP:08/31/2019 L.03/2017 EXP:03/31/2020 L.06/2017 EXP:06/30/2020 L.07/2017- EXP:07/31/2020 L.11/2017 EXP:11/30/2020 250ML L.01/2016 EXP:01/31/2019 L.06/2016 EXP:06/30/2019 L.08/2017 EXP:08/31/2020 |
Distribution
- AZ
- CA
- CO
- CT
- HI
- ID
- IL
- LA
- MA
- ME
- MI
- MN
- OH
- OK.
- PA
- RI
- SC
- TN
- UT
- VA
- WA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0698-2018
- Event ID
- 79056
- Status
- Terminated
- Classification
- Class II
- Company
- Manicaretti Inc
- Product description
- IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT; 100 ml and 250 ml sizes; UPC 100 ml - 7 93232 54200 3; UPC 250 ml - 7 93232 54203 4 Ingredients: Anchovies, Salt, Water. Product of Italy. Produced by ISA srl Pellezzano (SA)
- Quantity
- 811 CS FOR 100ML AND 101 CS FOR 250ML (6 units per case)
- Reason
- Rapid Alert System for Food and Feed notification received from Italy regarding high histamine levels in imported anchovy sauce.
- Recall initiation date
- January 12, 2018
- Report date
- February 7, 2018
- Classification date
- Not published in this source record
- Termination date
- May 8, 2018
- Distribution pattern
- AZ, CA, CO, CT, HI, ID, IL, LA, MA, ME, MI, MN, OH, OK., PA, RI, SC, TN, UT, VA, WA
- UPC, lot, and code information
- 100ML L.11/2015 EXP:11/30/2018 L.08/2016 EXP:08/31/2019 L.03/2017 EXP:03/31/2020 L.06/2017 EXP:06/30/2020 L.07/2017- EXP:07/31/2020 L.11/2017 EXP:11/30/2020 250ML L.01/2016 EXP:01/31/2019 L.06/2016 EXP:06/30/2019 L.08/2017 EXP:08/31/2020
- 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: Manicaretti Inc
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 |
|---|---|
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Hawaii | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 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.
