Productos Mdm
FDA import alert and refusal historyGarza Garcia, MexicoFEI 3017380211
Recorded by FDA as PRODUCTOS MDM
As of October 26, 2026, Productos Mdm is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines on January 5, 2021, most often for processor not registered for canned or acidified foods (NEEDS FCE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Pastes, n.e.c. · NEEDS FCE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Productos Mdm
7 records, newest first. Each line links to the FDA page it came from.
2021
- Import refusalSource
Refused, 7 lines in one entry: Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Show 7 linesHide lines
- Refused, Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Source
- Refused, Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Source
- Refused, Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Source
- Refused, Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Source
- Refused, Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Source
- Refused, Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Source
- Refused, Pastes, n.e.c.NEEDS FCENO PROCESSEntry 92F-0017246-1Source
Refusal charges, in plain English
- NEEDS FCE7 refused lines
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
- NO PROCESS7 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Productos Mdm
- Is Productos Mdm on an FDA import alert?
- No listing for Productos Mdm appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Productos Mdm?
- Yes. FDA refused 7 shipment lines from Productos Mdm on January 5, 2021. The most recent, on January 5, 2021, was pastes, n.e.c., charged as NEEDS FCE (processor not registered for canned or acidified foods).
- Why did FDA refuse Productos Mdm's shipments?
- The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 7 lines) and NO PROCESS (no scheduled process filed, 7 lines).
- What is Productos Mdm's FEI number?
- Productos Mdm's FDA Establishment Identifier (FEI) is 3017380211.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.