Emmanuel Mandez Barrios
FDA import alert and refusal historyReynosa, MexicoFEI 3005088669
As of October 25, 2026, Emmanuel Mandez Barrios (Reynosa, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for squash, summer (fruit used as vegetable), raw, fresh, ambient; squash, summer (fruit used as vegetable), raw, fresh, refrigerated, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Emmanuel Mandez Barrios
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listSquash, Summer (Fruit Used as Vegetable), Raw, Fresh, Ambient; Squash, Summer (Fruit Used as Vegetable), Raw, Fresh, RefrigeratedSource
Questions about Emmanuel Mandez Barrios
- Is Emmanuel Mandez Barrios on an FDA import alert?
- Yes. As of October 25, 2026, Emmanuel Mandez Barrios is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for squash, summer (fruit used as vegetable), raw, fresh, ambient; squash, summer (fruit used as vegetable), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Emmanuel Mandez Barrios?
- No FDA import refusals for Emmanuel Mandez Barrios appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Emmanuel Mandez Barrios's FEI number?
- Emmanuel Mandez Barrios's FDA Establishment Identifier (FEI) is 3005088669.
- Can shipments from Emmanuel Mandez Barrios still enter the U.S.?
- Shipments of squash, summer (fruit used as vegetable), raw, fresh, ambient; squash, summer (fruit used as vegetable), raw, fresh, refrigerated from Emmanuel Mandez Barrios can be detained without physical examination under Import Alert 99-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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