FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I
Thomson International, Inc.
- Product
- Sweet Yellow onions; Packed under brand names of Thomson Pr…
- Published
- September 2, 2020
- Distribution
- Nationwide
United States
TerminatedClass I
Traceback investigation into an outbreak of Salmonella Newport illnesses found red onions to be a suspect vehicle for the outbreak. After notification from FDA, firm initiated a recall.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Red onions; Packed under brand names of Thomson Premium, Onions 52, Utah Onions, Harley's Best, Onions 52, Imperial Fresh, TLC Thomson International, El Competidor Thomson Premium packed in 50 and 25 lb.mesh sack, and 2 lb. mesh sack - UPC 33383 60101 3 lb. mesh sack - UPC 33383 60102 TLC International - 40 lbs. carton - no UPC Utah onions 8 lb. mesh sack - Do not currently have UPC; Hatley's Best 8 lb. mesh sack - UPC 0 33383 60004 8 Imperial Fresh in 25 lb. mesh sack, 50, 25, 10 and 5 lb. cartons - 25 lb. Carton (Sysco/Freshpoint - carton UPC 0 00 74865 52351 6 Onions 52 - 2 lbs. mesh sack, UPC 0 33383 60101 | Not published in this source record | 18,750 tons - all varieties | ALL CODES- shipped from May 1, 2020 to present Lot Codes: 533-543-553-563-450 |
This recall shares FDA event ID 86156 with 3 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I
FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I
FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I
Responsible company: Thomson International, Inc.
FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I
FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I
FDA Recall United States TerminatedTerminated: September 28, 2020Historical recordClass I
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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.
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
This record is preserved as published by FDA, as of September 28, 2020.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.
Reconnecting to the server…
We lost the connection to the server.
Your session has expired.