Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported May 22, 2019
Vega White Headless Shrimp, 21/15 and 26/30 count size. Frozen block in plastic bag, 6 x 4 lbs. per master carton. Product of the Philippines Processed and Packed by HJR International Corp.
FDA import sample found Salmonella poly D in White Headless Shrimp- lot not released. Firm is recalling two additional lots as they are from the same packer and were received in t…
Union Fish Company recalled Vega White Headless Shrimp, 21/15 and 26/30 count size. Frozen block in plastic bag, 6 x… — a moderate-severity action.
Vega White Headless Shrimp, 21/15 and 26/30 count size. Frozen block in plastic bag, 6 x… was recalled by Union Fish Company in May 22, 2019. Reason: FDA import sample found Salmonella poly D in White Headless Shrimp- lot not released. Firm is recalling two a…. Check the official notice for the remedy. Verify recall #F-1341-2019 with the FDA Food before acting.
The recall
Union Fish Company issued this moderate-severity FDA Food recall — FDA import sample found Salmonella poly D in White Headless Shrimp- lot not released. Firm is recalling two a….
- Moderate
- severity level
- Class II
- classification
- May 22, 2019
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1341-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1341-2019) was formally reported on May 22, 2019, with the manufacturer initiating the action on March 18, 2019. It is classified under Moderate severity (Class II), with a current status of Terminated. Union Fish Company is listed as the recalling firm, operating out of Larkspur, CA. Federal records list the affected scope as 2400 lbs..
The documented reason for this recall is: FDA import sample found Salmonella poly D in White Headless Shrimp- lot not released. Firm is recalling two additional lots as they are from the same packer and were received in the same import entry. Distribution data in the federal record shows the product reached: CA, HI. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Vehicles recalls over time
Where this recall sits in its category — 9,301 vehicles recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
2400 lbs.
Related Recalls
6
2 from same agency
Product description
Vega White Headless Shrimp, 21/15 and 26/30 count size. Frozen block in plastic bag, 6 x 4 lbs. per master carton. Product of the Philippines Processed and Packed by HJR International Corp.
Reason for recall
FDA import sample found Salmonella poly D in White Headless Shrimp- lot not released. Firm is recalling two additional lots as they are from the same packer and were received in the same import entry.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1341-2019 |
| Date reported | May 22, 2019 |
| Date initiated | March 18, 2019 |
| Recalling firm | Union Fish Company |
| Firm location | Larkspur, CA |
| Affected scope | 2400 lbs. |
| Distribution | CA, HI |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1341-2019) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting — recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Vega White Headless Shrimp, 21/15 and 26/30 count size. Frozen block in plastic bag, 6 x 4 lbs. per master carton. Product of the Philippines Processed and Packed by HJR International Corp.. Recalled by Union Fish Company. Units affected: 2400 lbs..
Why was this product recalled? ▼
FDA import sample found Salmonella poly D in White Headless Shrimp- lot not released. Firm is recalling two additional lots as they are from the same packer and were received in the same import entry.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 22, 2019. Severity: Moderate. Recall number: F-1341-2019.
Where was the recalled product distributed? ▼
Distribution: CA, HI.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1341-2019) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Continue exploring
Keep tracking product safety across the federal recall archive.
Recall Checker
Search the full archive by product name, brand, or recall number across every agency.
Check a product →
FDA Food recalls
Every recall issued by FDA Food, newest first.
Browse the feed →
RecallRadar
Live feed of the latest recalls across the FDA, CPSC and NHTSA — filter by agency and severity.
View the live feed →
Rankings
The largest recalls by units affected and the most-recalled product categories.
See the rankings →
Browse by category
Find recalls by product type to spot recurring defect patterns.
All categories →
What to do next
A step-by-step guide to refunds, repairs, and returns after a recall.
Read the guide →
Nearby Recalls in This Category
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
FDA Drug Moderate
Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distributed by: Haleon, Warren, NJ 07059, UPC: 3 00674 35041 9.
Haleon US Holdings LLC · 2026-05-27
FDA Food Low
Garland Fresh Peeled Garlic 6 oz. bag
Tops Markets LLC · 2026-05-13
FDA Food Low
Christopher Ranch Peeled Garlic 6 oz.
Tops Markets LLC · 2026-05-13
FDA Drug Moderate
BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 f…
CareFusion 213, LLC · 2026-05-13
FDA Drug Moderate
BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26m…
CareFusion 213, LLC · 2026-05-13
Compare this recall with Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distribut… →
Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported May 22, 2019.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.